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.
DEAFNESS, AUTOSOMAL RECESSIVE 89
National Institutes of Health
Autosomal recessive inheritance
Semantic Scholar uses AI to extract papers important to this topic.
DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2
S. M. Leal
Corpus ID: 9731086
DFNB89 is a novel autosomal recessive nonsyndromic hearing impairment (ARNSHI) locus that was mapped to 16q21-q23.2. Linkage to…
Is this relevant?
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Terms of Service
ACCEPT & CONTINUE