## 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
Diverse polymorphism within a short coding region of the human aldehyde dehydrogenase-5 (ALDH5) gene
✍ Scribed by David Sherman; Vibha Davé; Lily C. Hsu; Timothy J. Peters; Akira Yoshida
- Publisher
- Springer
- Year
- 1993
- Tongue
- English
- Weight
- 471 KB
- Volume
- 92
- Category
- Article
- ISSN
- 0340-6717
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