ISSN:
1546-1718
Source:
Nature Archives 1869 - 2009
Topics:
Biology
,
Medicine
Notes:
[Auszug] Usher syndrome type 1 (USH1) is an autosomal recessive sensory defect involving congenital profound sensorineural deafness, vestibular dysfunction and blindness (due to progressive retinitis pigmentosa). Six different USH1 loci have been reported. So far, only MYO7A (USH1B), encoding myosin ...
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1038/79171
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