Skip to search form
Skip to main content
Semantic Scholar's Logo
Create Free Account
You are currently offline. Some features of the site may not work correctly.
National Institutes of Health
USHER SYNDROME, TYPE IB (disorder)
Semantic Scholar uses AI to extract papers important to this topic.
Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients.
M. D. Weston
P. M. Kelley
American journal of human genetics
Corpus ID: 2340288
Usher syndrome type 1b (USH1B) is an autosomal recessive disorder characterized by congenital profound hearing loss, vestibular…
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Terms of Service
ACCEPT & CONTINUE