Genotype and phenotype variability in Sjögren‐Larsson syndrome
M Weustenfeld, R Eidelpes, M Schmuth… - Human …, 2019 - Wiley Online Library
Abstract The Sjögren–Larsson syndrome (SLS) is a rare autosomal recessive disorder
caused by pathogenic variants in the ALDH3A2 gene, which codes for fatty aldehyde …
caused by pathogenic variants in the ALDH3A2 gene, which codes for fatty aldehyde …
Genotype and phenotype variability in Sjögren-Larsson syndrome.
M Weustenfeld, R Eidelpes, M Schmuth, WB Rizzo… - Human …, 2018 - europepmc.org
Abstract The Sjögren–Larsson syndrome (SLS) is a rare autosomal recessive disorder
caused by pathogenic variants in the ALDH3A2 gene, which codes for fatty aldehyde …
caused by pathogenic variants in the ALDH3A2 gene, which codes for fatty aldehyde …
[HTML][HTML] Genotype and phenotype variability in Sjögren‐Larsson syndrome
M Weustenfeld, R Eidelpes, M Schmuth… - Human …, 2019 - ncbi.nlm.nih.gov
Abstract The Sjögren–Larsson syndrome (SLS) is a rare autosomal recessive disorder
caused by pathogenic variants in the ALDH3A2 gene, which codes for fatty aldehyde …
caused by pathogenic variants in the ALDH3A2 gene, which codes for fatty aldehyde …
Genotype and phenotype variability in Sjögren-Larsson syndrome
M Weustenfeld, R Eidelpes, M Schmuth… - Human …, 2019 - pubmed.ncbi.nlm.nih.gov
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 …
pathogenic variants in the ALDH3A2 gene, which codes for fatty aldehyde dehydrogenase …
Genotype and phenotype variability in Sjogren-Larsson syndrome
M Weustenfeld, R Eidelpes, M Schmuth, WB Rizzo… - Human …, 2019 - hero.epa.gov
Abstract The Sjogren-Larsson syndrome (SLS) is a rare autosomal recessive disorder
caused by pathogenic variants in the ALDH3A2 gene, which codes for fatty aldehyde …
caused by pathogenic variants in the ALDH3A2 gene, which codes for fatty aldehyde …
Genotype and phenotype variability in Sjögren-Larsson syndrome
M Weustenfeld, R Eidelpes, M Schmuth… - Human …, 2019 - experts.nebraska.edu
Abstract The Sjögren–Larsson syndrome (SLS) is a rare autosomal recessive disorder
caused by pathogenic variants in the ALDH3A2 gene, which codes for fatty aldehyde …
caused by pathogenic variants in the ALDH3A2 gene, which codes for fatty aldehyde …
Genotype and phenotype variability in Sjögren-Larsson syndrome.
M Weustenfeld, R Eidelpes, M Schmuth, WB Rizzo… - Human …, 2018 - europepmc.org
Abstract The Sjögren–Larsson syndrome (SLS) is a rare autosomal recessive disorder
caused by pathogenic variants in the ALDH3A2 gene, which codes for fatty aldehyde …
caused by pathogenic variants in the ALDH3A2 gene, which codes for fatty aldehyde …