Genetic heterogeneity of Usher syndrome type II.

Usher syndrome is an autosomal recessive disorder characterised by retinitis pigmentosa and congenital sensorineural hearing loss. A gene for Usher syndrome type II (USH2) has been localised to chromosome 1q32-q41. DNA from a family with four of seven sibs affected with clinical characteristics of U...

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Autors principals: Pieke Dahl, S, Kimberling, W J, Gorin, M B, Weston, M D, Furman, J M, Pikus, A, Möller, C
Format: Artigo
Idioma:Inglês
Publicat: 1993
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1016567/
https://ncbi.nlm.nih.gov/pubmed/7901420
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