Long-Chain Fatty Acid Oxidation Disorder Genes: A Comprehensive Genetic Database of LC-FAOD Variants, Genotypes, and Phenotypes.
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| Title: | Long-Chain Fatty Acid Oxidation Disorder Genes: A Comprehensive Genetic Database of LC-FAOD Variants, Genotypes, and Phenotypes. |
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| Authors: | Richbourg H; Ultragenyx Pharmaceutical Inc., Novato, California, USA., Rangel Miller V; Ultragenyx Pharmaceutical Inc., Novato, California, USA., Khazaie Japalaghi O; Ultragenyx Pharmaceutical Inc., Novato, California, USA., AlSayed M; College of Medicine, Al-Faisal University, Riyadh, Riyadh Province, Saudi Arabia, alfaisal.edu., Baker PR; Anschutz Medical Campus, University of Colorado, Aurora, Colorado, USA, colorado.edu., Daugherty S; Ultragenyx Pharmaceutical Inc., Novato, California, USA., Ekstein T; Labcorp, San Francisco, California, USA., Grünert SC; Children's Hospital, Department of Pediatrics, Adolescent Medicine and Neonatology, Faculty of Medicine, Freiburg University Hospital, Freiburg, Baden-Württemberg, Germany., Kiel MJ; Genomenon, Ann Arbor, Michigan, USA., Khan A; M.A.G.I.C. (Metabolics and Genetics in Canada) Clinic Ltd., Calgary, Alberta, Canada., Kobayashi H; Laboratories Division, Shimane University Hospital, Izumo, Shimane Prefecture, Japan, shimane-u.ac.jp., Korngut L; Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada, ucalgary.ca., Monteleone SA; Genomenon, Ann Arbor, Michigan, USA., Schwartz IVD; Hospital de Clinicas, Porto Alegre, Rio Grande do Sul, Brazil., Miller N; Ultragenyx Pharmaceutical Inc., Novato, California, USA., Vockley J; Division of Medical Genetics and Center for Rare Disease Therapy, University of Pittsburgh, Pittsburgh, Pennsylvania, USA, pitt.edu. |
| Source: | Human mutation [Hum Mutat] 2026 Jul 07; Vol. 2026, pp. 6864813. Date of Electronic Publication: 2026 Jul 07 (Print Publication: 2026). |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: eCollection Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 42422157 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Long-Chain Fatty Acid Oxidation Disorder Genes: A Comprehensive Genetic Database of LC-FAOD Variants, Genotypes, and Phenotypes. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Richbourg+H%22">Richbourg H</searchLink>; Ultragenyx Pharmaceutical Inc., Novato, California, USA.<br /><searchLink fieldCode="AU" term="%22Rangel+Miller+V%22">Rangel Miller V</searchLink>; Ultragenyx Pharmaceutical Inc., Novato, California, USA.<br /><searchLink fieldCode="AU" term="%22Khazaie+Japalaghi+O%22">Khazaie Japalaghi O</searchLink>; Ultragenyx Pharmaceutical Inc., Novato, California, USA.<br /><searchLink fieldCode="AU" term="%22AlSayed+M%22">AlSayed M</searchLink>; College of Medicine, Al-Faisal University, Riyadh, Riyadh Province, Saudi Arabia, alfaisal.edu.<br /><searchLink fieldCode="AU" term="%22Baker+PR%22">Baker PR</searchLink>; Anschutz Medical Campus, University of Colorado, Aurora, Colorado, USA, colorado.edu.<br /><searchLink fieldCode="AU" term="%22Daugherty+S%22">Daugherty S</searchLink>; Ultragenyx Pharmaceutical Inc., Novato, California, USA.<br /><searchLink fieldCode="AU" term="%22Ekstein+T%22">Ekstein T</searchLink>; Labcorp, San Francisco, California, USA.<br /><searchLink fieldCode="AU" term="%22Grünert+SC%22">Grünert SC</searchLink>; Children's Hospital, Department of Pediatrics, Adolescent Medicine and Neonatology, Faculty of Medicine, Freiburg University Hospital, Freiburg, Baden-Württemberg, Germany.<br /><searchLink fieldCode="AU" term="%22Kiel+MJ%22">Kiel MJ</searchLink>; Genomenon, Ann Arbor, Michigan, USA.<br /><searchLink fieldCode="AU" term="%22Khan+A%22">Khan A</searchLink>; M.A.G.I.C. (Metabolics and Genetics in Canada) Clinic Ltd., Calgary, Alberta, Canada.<br /><searchLink fieldCode="AU" term="%22Kobayashi+H%22">Kobayashi H</searchLink>; Laboratories Division, Shimane University Hospital, Izumo, Shimane Prefecture, Japan, shimane-u.ac.jp.<br /><searchLink fieldCode="AU" term="%22Korngut+L%22">Korngut L</searchLink>; Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada, ucalgary.ca.<br /><searchLink fieldCode="AU" term="%22Monteleone+SA%22">Monteleone SA</searchLink>; Genomenon, Ann Arbor, Michigan, USA.<br /><searchLink fieldCode="AU" term="%22Schwartz+IVD%22">Schwartz IVD</searchLink>; Hospital de Clinicas, Porto Alegre, Rio Grande do Sul, Brazil.<br /><searchLink fieldCode="AU" term="%22Miller+N%22">Miller N</searchLink>; Ultragenyx Pharmaceutical Inc., Novato, California, USA.<br /><searchLink fieldCode="AU" term="%22Vockley+J%22">Vockley J</searchLink>; Division of Medical Genetics and Center for Rare Disease Therapy, University of Pittsburgh, Pittsburgh, Pennsylvania, USA, pitt.edu. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229215429%22">Human mutation</searchLink> [Hum Mutat] 2026 Jul 07; Vol. 2026, pp. 6864813. <i>Date of Electronic Publication: </i>2026 Jul 07 (<i>Print Publication: </i>2026). – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Liss%22">Wiley-Liss </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9215429 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Internet <i>ISSN: </i>1098-1004 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210597794%22">10597794 </searchLink><i>NLM ISO Abbreviation: </i>Hum Mutat <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=42422157 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1155/humu/6864813 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 6864813 Titles: – TitleFull: Long-Chain Fatty Acid Oxidation Disorder Genes: A Comprehensive Genetic Database of LC-FAOD Variants, Genotypes, and Phenotypes. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Richbourg H – PersonEntity: Name: NameFull: Rangel Miller V – PersonEntity: Name: NameFull: Khazaie Japalaghi O – PersonEntity: Name: NameFull: AlSayed M – PersonEntity: Name: NameFull: Baker PR – PersonEntity: Name: NameFull: Daugherty S – PersonEntity: Name: NameFull: Ekstein T – PersonEntity: Name: NameFull: Grünert SC – PersonEntity: Name: NameFull: Kiel MJ – PersonEntity: Name: NameFull: Khan A – PersonEntity: Name: NameFull: Kobayashi H – PersonEntity: Name: NameFull: Korngut L – PersonEntity: Name: NameFull: Monteleone SA – PersonEntity: Name: NameFull: Schwartz IVD – PersonEntity: Name: NameFull: Miller N – PersonEntity: Name: NameFull: Vockley J IsPartOfRelationships: – BibEntity: Dates: – D: 07 M: 07 Text: 2026 Jul 07 Type: published Y: 2026 Identifiers: – Type: issn-electronic Value: 1098-1004 Numbering: – Type: volume Value: 2026 Titles: – TitleFull: Human mutation Type: main |
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