Linkage analysis in Usher syndrome type I (USH1) families from Spain.

Usher syndrome (USH) is an autosomal recessive hereditary disorder characterised by congenital sensorineural hearing loss and gradual visual impairment secondary to retinitis pigmentosa (RP). The disorder is clinically and genetically heterogeneous. With regard to Usher type I (USH1), several subtyp...

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Autors principals: Espinós, C, Nájera, C, Millán, J M, Ayuso, C, Baiget, M, Pérez-Garrigues, H, Rodrigo, O, Vilela, C, Beneyto, M
Format: Artigo
Idioma:Inglês
Publicat: 1998
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051313/
https://ncbi.nlm.nih.gov/pubmed/9610802
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