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Autosomal Recessive Nonsyndromic Deafness 53
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 COL11A2 gene on chromosome 6p21.
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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 COL11A2 gene on chromosome 6p21.
Resources
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