Genetic Polymorphism of Aldehyde Dehydrogenase 2 (ALDH2) in a Chinese Population: Gender, Age, Culture, and Genotypes ofALDH2

Sjögren-Larsson syndrome: Diversity of m

Sjögren-Larsson syndrome: Diversity of mutations and polymorphisms in the fatty aldehyde dehydrogenase gene (ALDH3A2)

✍ William B. Rizzo; Gael Carney 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 228 KB

## Communicated by Jan P. Kraus Sjo ¨gren-Larsson syndrome (SLS) is an autosomal recessive disorder characterized by ichthyosis, mental retardation, and spastic diplegia or tetraplegia. The disease is caused by mutations in the ALDH3A2 gene (also known as FALDH and ALDH10) on chromosome 17p11.2 th