Genetic homogeneity in Sjögren-Larsson syndrome: linkage to chromosome 17p in families of different non-Swedish ethnic origins.

Sjögren-Larsson syndrome (SLS) is a rare, autosomal recessive disorder that is characterized by congenital ichthyosis, mental retardation, and spastic diplegia or tetraplegia. Three United States families, three Egyptian families, and one Israeli Arab family were investigated for linkage of the SLS...

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Библиографические подробности
Главные авторы: Rogers, G R, Rizzo, W B, Zlotogorski, A, Hashem, N, Lee, M, Compton, J G, Bale, S J
Формат: Artigo
Язык:Inglês
Опубликовано: 1995
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Research Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC1801386/
https://ncbi.nlm.nih.gov/pubmed/7485163
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