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DEAFNESS, AUTOSOMAL RECESSIVE 13
National Institutes of Health
Autosomal recessive inheritance
Sensorineural Hearing Loss (disorder)
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A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36
European Journal of Human Genetics
Corpus ID: 8846019
Deafness is the most frequent sensorineural defect in children. The vast majority of the prelingual forms of isolated deafness…
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