Genetic heterogeneity of Usher syndrome type II in a Dutch population.

The Usher syndromes are a group of autosomal recessive disorders characterised by retinitis pigmentosa (RP) with congenital, stable (non-progressive) sensorineural hearing loss. Profound deafness, RP, and no vestibular responses are features of Usher type I, whereas moderate to severe hearing loss a...

Full description

Saved in:
Bibliographic Details
Main Authors: Pieke-Dahl, S, van Aarem, A, Dobin, A, Cremers, C W, Kimberling, W J
Format: Artigo
Language:Inglês
Published: 1996
Subjects:
Research Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1050729/
https://ncbi.nlm.nih.gov/pubmed/8880575
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items