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Autosomal Recessive Nonsyndromic Deafness 63
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and is caused by mutation in the LRTOMT gene on chromosome 11q13.
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When to seek help
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Overview
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and is caused by mutation in the LRTOMT gene on chromosome 11q13.
Resources
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