The Molecular Basis of Sjögren-Larsson Syndrome: Mutation Analysis of the Fatty Aldehyde Dehydrogenase Gene
- 1 December 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 65 (6) , 1547-1560
- https://doi.org/10.1086/302681
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Relationships within the aldehyde dehydrogenase extended familyProtein Science, 1999
- A missense mutation in the FALDH gene identified in Sjögren-Larsson syndrome patients originating from the northern part of SwedenHuman Genetics, 1997
- Mutations associated with Sjögren–Larsson SyndromeAnnals of Human Genetics, 1997
- Human Fatty Aldehyde Dehydrogenase Gene (ALDH10): Organization and Tissue-Dependent ExpressionGenomics, 1997
- Genomic Organization and Expression of the Human Fatty Aldehyde Dehydrogenase Gene (FALDH)Genomics, 1997
- Confirmation of linkage of Sjogren-Larsson syndrome to chromosome 17 in families of different ethnic origins.Journal of Medical Genetics, 1996
- Sjögren–Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase geneNature Genetics, 1996
- The Sjögren-Larsson Syndrome gene is close to D17S805 as determined by linkage analysis and allelic associationNature Genetics, 1994
- Multiplex PCR amplification from the CFTR gene using DNA prepared from buccal brushes/swabsHuman Molecular Genetics, 1993
- Sjögren-Larsson syndrome. Impaired fatty alcohol oxidation in cultured fibroblasts due to deficient fatty alcohol:nicotinamide adenine dinucleotide oxidoreductase activity.Journal of Clinical Investigation, 1988