A novel pathogenic ATP6V1B2 variant: Widening the genotypic spectrum of the epileptic neurodevelopmental phenotype.
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| Title: | A novel pathogenic ATP6V1B2 variant: Widening the genotypic spectrum of the epileptic neurodevelopmental phenotype. |
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| Authors: | Veltra D; Laboratory of Medical Genetics, School of Medicine, National & Kapodistrian University of Athens, 'St. Sophia's' Children's Hospital, Athens, Greece., Kosma K; Laboratory of Medical Genetics, School of Medicine, National & Kapodistrian University of Athens, 'St. Sophia's' Children's Hospital, Athens, Greece., Papavasiliou A; Department of Pediatric Neurology, Iaso Children's Hospital, Marousi, Greece., Tilemis FN; Laboratory of Medical Genetics, School of Medicine, National & Kapodistrian University of Athens, 'St. Sophia's' Children's Hospital, Athens, Greece.; Research University Institute for the Study of Genetic and Malignant Disease of Childhood, 'St. Sophia's' Children's Hospital, Athens, Greece., Traeger-Synodinos J; Laboratory of Medical Genetics, School of Medicine, National & Kapodistrian University of Athens, 'St. Sophia's' Children's Hospital, Athens, Greece., Sofocleous C; Laboratory of Medical Genetics, School of Medicine, National & Kapodistrian University of Athens, 'St. Sophia's' Children's Hospital, Athens, Greece.; Research University Institute for the Study of Genetic and Malignant Disease of Childhood, 'St. Sophia's' Children's Hospital, Athens, Greece. |
| Source: | American journal of medical genetics. Part A [Am J Med Genet A] 2022 Dec; Vol. 188 (12), pp. 3563-3566. Date of Electronic Publication: 2022 Sep 22. |
| Publication Type: | Case Reports; Journal Article |
| Journal Info: | Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 36135319 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: A novel pathogenic ATP6V1B2 variant: Widening the genotypic spectrum of the epileptic neurodevelopmental phenotype. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Veltra+D%22">Veltra D</searchLink>; Laboratory of Medical Genetics, School of Medicine, National & Kapodistrian University of Athens, 'St. Sophia's' Children's Hospital, Athens, Greece.<br /><searchLink fieldCode="AU" term="%22Kosma+K%22">Kosma K</searchLink>; Laboratory of Medical Genetics, School of Medicine, National & Kapodistrian University of Athens, 'St. Sophia's' Children's Hospital, Athens, Greece.<br /><searchLink fieldCode="AU" term="%22Papavasiliou+A%22">Papavasiliou A</searchLink>; Department of Pediatric Neurology, Iaso Children's Hospital, Marousi, Greece.<br /><searchLink fieldCode="AU" term="%22Tilemis+FN%22">Tilemis FN</searchLink>; Laboratory of Medical Genetics, School of Medicine, National & Kapodistrian University of Athens, 'St. Sophia's' Children's Hospital, Athens, Greece.; Research University Institute for the Study of Genetic and Malignant Disease of Childhood, 'St. Sophia's' Children's Hospital, Athens, Greece.<br /><searchLink fieldCode="AU" term="%22Traeger-Synodinos+J%22">Traeger-Synodinos J</searchLink>; Laboratory of Medical Genetics, School of Medicine, National & Kapodistrian University of Athens, 'St. Sophia's' Children's Hospital, Athens, Greece.<br /><searchLink fieldCode="AU" term="%22Sofocleous+C%22">Sofocleous C</searchLink>; Laboratory of Medical Genetics, School of Medicine, National & Kapodistrian University of Athens, 'St. Sophia's' Children's Hospital, Athens, Greece.; Research University Institute for the Study of Genetic and Malignant Disease of Childhood, 'St. Sophia's' Children's Hospital, Athens, Greece. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101235741%22">American journal of medical genetics. Part A</searchLink> [Am J Med Genet A] 2022 Dec; Vol. 188 (12), pp. 3563-3566. <i>Date of Electronic Publication: </i>2022 Sep 22. – Name: TypePub Label: Publication Type Group: TypPub Data: Case Reports; Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Blackwell%22">Wiley-Blackwell </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101235741 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1552-4833 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2215524825%22">15524825 </searchLink><i>NLM ISO Abbreviation: </i>Am J Med Genet A <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=36135319 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/ajmg.a.62971 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 3563 Titles: – TitleFull: A novel pathogenic ATP6V1B2 variant: Widening the genotypic spectrum of the epileptic neurodevelopmental phenotype. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Veltra D – PersonEntity: Name: NameFull: Kosma K – PersonEntity: Name: NameFull: Papavasiliou A – PersonEntity: Name: NameFull: Tilemis FN – PersonEntity: Name: NameFull: Traeger-Synodinos J – PersonEntity: Name: NameFull: Sofocleous C IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 12 Text: 2022 Dec Type: published Y: 2022 Identifiers: – Type: issn-electronic Value: 1552-4833 Numbering: – Type: volume Value: 188 – Type: issue Value: 12 Titles: – TitleFull: American journal of medical genetics. Part A Type: main |
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