A homozygous missense variant in CHRM3 associated with familial urinary bladder disease.
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| Title: | A homozygous missense variant in CHRM3 associated with familial urinary bladder disease. |
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| Authors: | Beaman GM; Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Human Sciences, University of Manchester, Manchester, UK., Galatà G; Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Human Sciences, University of Manchester, Manchester, UK., Teik KW; Department of Genetics, Hospital Kuala Lumpur, Kuala Lumpur, Malaysia., Urquhart JE; Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Human Sciences, University of Manchester, Manchester, UK., Aishah A; Department of Genetics, Hospital Kuala Lumpur, Kuala Lumpur, Malaysia., O'Sullivan J; Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Human Sciences, University of Manchester, Manchester, UK., Bhaskar SS; Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Human Sciences, University of Manchester, Manchester, UK., Wood KA; Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Human Sciences, University of Manchester, Manchester, UK., Thomas HB; Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Human Sciences, University of Manchester, Manchester, UK., O'Keefe RT; Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Human Sciences, University of Manchester, Manchester, UK., Woolf AS; Division of Cell Matrix Biology and Regenerative Medicine, School of Biological Sciences, Faculty of Biology Medicine and Health, University of Manchester, Manchester, UK.; Royal Manchester Children's Hospital, Manchester University NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK., Stuart HM; Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Human Sciences, University of Manchester, Manchester, UK., Newman WG; Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Human Sciences, University of Manchester, Manchester, UK.; Peking University Health Sciences Center, Beijing, China. |
| Source: | Clinical genetics [Clin Genet] 2019 Dec; Vol. 96 (6), pp. 515-520. Date of Electronic Publication: 2019 Sep 11. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 31441039 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: A homozygous missense variant in CHRM3 associated with familial urinary bladder disease. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Beaman+GM%22">Beaman GM</searchLink>; Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Human Sciences, University of Manchester, Manchester, UK.<br /><searchLink fieldCode="AU" term="%22Galatà+G%22">Galatà G</searchLink>; Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Human Sciences, University of Manchester, Manchester, UK.<br /><searchLink fieldCode="AU" term="%22Teik+KW%22">Teik KW</searchLink>; Department of Genetics, Hospital Kuala Lumpur, Kuala Lumpur, Malaysia.<br /><searchLink fieldCode="AU" term="%22Urquhart+JE%22">Urquhart JE</searchLink>; Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Human Sciences, University of Manchester, Manchester, UK.<br /><searchLink fieldCode="AU" term="%22Aishah+A%22">Aishah A</searchLink>; Department of Genetics, Hospital Kuala Lumpur, Kuala Lumpur, Malaysia.<br /><searchLink fieldCode="AU" term="%22O'Sullivan+J%22">O'Sullivan J</searchLink>; Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Human Sciences, University of Manchester, Manchester, UK.<br /><searchLink fieldCode="AU" term="%22Bhaskar+SS%22">Bhaskar SS</searchLink>; Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Human Sciences, University of Manchester, Manchester, UK.<br /><searchLink fieldCode="AU" term="%22Wood+KA%22">Wood KA</searchLink>; Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Human Sciences, University of Manchester, Manchester, UK.<br /><searchLink fieldCode="AU" term="%22Thomas+HB%22">Thomas HB</searchLink>; Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Human Sciences, University of Manchester, Manchester, UK.<br /><searchLink fieldCode="AU" term="%22O'Keefe+RT%22">O'Keefe RT</searchLink>; Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Human Sciences, University of Manchester, Manchester, UK.<br /><searchLink fieldCode="AU" term="%22Woolf+AS%22">Woolf AS</searchLink>; Division of Cell Matrix Biology and Regenerative Medicine, School of Biological Sciences, Faculty of Biology Medicine and Health, University of Manchester, Manchester, UK.; Royal Manchester Children's Hospital, Manchester University NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK.<br /><searchLink fieldCode="AU" term="%22Stuart+HM%22">Stuart HM</searchLink>; Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Human Sciences, University of Manchester, Manchester, UK.<br /><searchLink fieldCode="AU" term="%22Newman+WG%22">Newman WG</searchLink>; Manchester Centre for Genomic Medicine, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.; Division of Evolution and Genomic Sciences, Faculty of Biology, Medicine and Human Sciences, University of Manchester, Manchester, UK.; Peking University Health Sciences Center, Beijing, China. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%220253664%22">Clinical genetics</searchLink> [Clin Genet] 2019 Dec; Vol. 96 (6), pp. 515-520. <i>Date of Electronic Publication: </i>2019 Sep 11. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Munksgaard%22">Munksgaard </searchLink><i>Country of Publication: </i>Denmark <i>NLM ID: </i>0253664 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1399-0004 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200099163%22">00099163 </searchLink><i>NLM ISO Abbreviation: </i>Clin Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=31441039 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/cge.13631 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 515 Titles: – TitleFull: A homozygous missense variant in CHRM3 associated with familial urinary bladder disease. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Beaman GM – PersonEntity: Name: NameFull: Galatà G – PersonEntity: Name: NameFull: Teik KW – PersonEntity: Name: NameFull: Urquhart JE – PersonEntity: Name: NameFull: Aishah A – PersonEntity: Name: NameFull: O'Sullivan J – PersonEntity: Name: NameFull: Bhaskar SS – PersonEntity: Name: NameFull: Wood KA – PersonEntity: Name: NameFull: Thomas HB – PersonEntity: Name: NameFull: O'Keefe RT – PersonEntity: Name: NameFull: Woolf AS – PersonEntity: Name: NameFull: Stuart HM – PersonEntity: Name: NameFull: Newman WG IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 12 Text: 2019 Dec Type: published Y: 2019 Identifiers: – Type: issn-electronic Value: 1399-0004 Numbering: – Type: volume Value: 96 – Type: issue Value: 6 Titles: – TitleFull: Clinical genetics Type: main |
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