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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Bibliografski detalji
Glavni autori: Rogers, G R, Rizzo, W B, Zlotogorski, A, Hashem, N, Lee, M, Compton, J G, Bale, S J
Format: Artigo
Jezik:Inglês
Izdano: 1995
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1801386/
https://ncbi.nlm.nih.gov/pubmed/7485163
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