D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia.
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| Title: | D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia. |
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| Authors: | Werner KM; Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA., Cox AJ; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.; PreventionGenetics LLC, Marshfield, Wisconsin, USA., Qian E; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA., Jain P; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.; Sema4, Stanford, CT, USA., Ji W; Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA., Tikhonova I; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA., Castaldi C; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA., Bilguvar K; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA., Knight J; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA., Ferdinandusse S; Department of Clinical Chemistry, Amsterdam UMC Locatie AMC, Amsterdam, Netherlands., Fawaz R; Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA., Jiang YH; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA., Gallagher PG; Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA.; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.; Department of Pathology, Yale University School of Medicine, New Haven, Connecticut, USA., Bizzarro M; Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA., Gruen JR; Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA.; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA., Bale A; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA., Zhang H; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA. |
| Source: | American journal of medical genetics. Part A [Am J Med Genet A] 2022 Jan; Vol. 188 (1), pp. 357-363. Date of Electronic Publication: 2021 Oct 08. |
| Publication Type: | Case Reports; Research Support, N.I.H., Extramural; 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: 34623748 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Werner+KM%22">Werner KM</searchLink>; Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA.<br /><searchLink fieldCode="AU" term="%22Cox+AJ%22">Cox AJ</searchLink>; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.; PreventionGenetics LLC, Marshfield, Wisconsin, USA.<br /><searchLink fieldCode="AU" term="%22Qian+E%22">Qian E</searchLink>; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.<br /><searchLink fieldCode="AU" term="%22Jain+P%22">Jain P</searchLink>; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.; Sema4, Stanford, CT, USA.<br /><searchLink fieldCode="AU" term="%22Ji+W%22">Ji W</searchLink>; Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA.<br /><searchLink fieldCode="AU" term="%22Tikhonova+I%22">Tikhonova I</searchLink>; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.<br /><searchLink fieldCode="AU" term="%22Castaldi+C%22">Castaldi C</searchLink>; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.<br /><searchLink fieldCode="AU" term="%22Bilguvar+K%22">Bilguvar K</searchLink>; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.<br /><searchLink fieldCode="AU" term="%22Knight+J%22">Knight J</searchLink>; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.<br /><searchLink fieldCode="AU" term="%22Ferdinandusse+S%22">Ferdinandusse S</searchLink>; Department of Clinical Chemistry, Amsterdam UMC Locatie AMC, Amsterdam, Netherlands.<br /><searchLink fieldCode="AU" term="%22Fawaz+R%22">Fawaz R</searchLink>; Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA.<br /><searchLink fieldCode="AU" term="%22Jiang+YH%22">Jiang YH</searchLink>; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.<br /><searchLink fieldCode="AU" term="%22Gallagher+PG%22">Gallagher PG</searchLink>; Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA.; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.; Department of Pathology, Yale University School of Medicine, New Haven, Connecticut, USA.<br /><searchLink fieldCode="AU" term="%22Bizzarro+M%22">Bizzarro M</searchLink>; Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA.<br /><searchLink fieldCode="AU" term="%22Gruen+JR%22">Gruen JR</searchLink>; Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA.; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.<br /><searchLink fieldCode="AU" term="%22Bale+A%22">Bale A</searchLink>; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.<br /><searchLink fieldCode="AU" term="%22Zhang+H%22">Zhang H</searchLink>; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA. – 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 Jan; Vol. 188 (1), pp. 357-363. <i>Date of Electronic Publication: </i>2021 Oct 08. – Name: TypePub Label: Publication Type Group: TypPub Data: Case Reports; Research Support, N.I.H., Extramural; 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=34623748 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/ajmg.a.62520 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 357 Titles: – TitleFull: D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Werner KM – PersonEntity: Name: NameFull: Cox AJ – PersonEntity: Name: NameFull: Qian E – PersonEntity: Name: NameFull: Jain P – PersonEntity: Name: NameFull: Ji W – PersonEntity: Name: NameFull: Tikhonova I – PersonEntity: Name: NameFull: Castaldi C – PersonEntity: Name: NameFull: Bilguvar K – PersonEntity: Name: NameFull: Knight J – PersonEntity: Name: NameFull: Ferdinandusse S – PersonEntity: Name: NameFull: Fawaz R – PersonEntity: Name: NameFull: Jiang YH – PersonEntity: Name: NameFull: Gallagher PG – PersonEntity: Name: NameFull: Bizzarro M – PersonEntity: Name: NameFull: Gruen JR – PersonEntity: Name: NameFull: Bale A – PersonEntity: Name: NameFull: Zhang H IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 01 Text: 2022 Jan Type: published Y: 2022 Identifiers: – Type: issn-electronic Value: 1552-4833 Numbering: – Type: volume Value: 188 – Type: issue Value: 1 Titles: – TitleFull: American journal of medical genetics. Part A Type: main |
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