Involvement of cochlin binding to sulfated heparan sulfate/heparin in the pathophysiology of autosomal dominant late-onset hearing loss (DFNA9)
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DOI: 10.1371/journal.pone.0268485
Abstract: Late-onset non-syndromic autosomal dominant hearing loss 9 (DFNA9) is a hearing impairment caused by mutations in the coagulation factor C homology gene (COCH). COCH encodes for cochlin, a major component of the cochlear extracellular matrix.… read more here.
Keywords: cochlin; hearing loss; autosomal dominant; loss dfna9 ... See more keywords