Genotype and phenotype variability in Sjögren‐Larsson syndrome
The Sjögren–Larsson syndrome (SLS) is a rare autosomal recessive disorder caused by pathogenic variants in the ALDH3A2 gene, which codes for fatty aldehyde dehydrogenase (FALDH). FALDH prevents the accumulation of toxic fatty aldehydes by converting them into fatty acids. Pathogenic ALDH3A2 variants...
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| Main Authors: | , , , , , |
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| Format: | Text |
| Language: | English |
| Published: |
John Wiley and Sons Inc.
2018
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| Subjects: | |
| Online Access: | https://pmc.ncbi.nlm.nih.gov/articles/PMC6587760/ https://pubmed.ncbi.nlm.nih.gov/30372562 http://dx.doi.org/10.1002/humu.23679 |
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