[In this study, seventy-five Iranian families segregating autosomal recessive non-syndromic hearing impairment were analyzed/sequencing all 23 coding exons of TECTA, a frameshift mutation was found.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
Gene-disease associations inferred from text-mining the literature.
DisGeNET evidence - LITERATURE