(Q28024587)
English
autosomal recessive nonsyndromic deafness 101
autosomal recessive nonsyndromic deafness that has material basis in mutation in the GRXCR2 gene on chromosome 5q32
- DFNB101
- autosomal recessive deafness 101
- DEAFNESS, AUTOSOMAL RECESSIVE 101
- autosomal recessive nonsyndromic deafness type 101
- Deafness, Autosomal Recessive type 101
- DEAFNESS, AUTOSOMAL RECESSIVE 101; DFNB101
Statements
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Identifiers
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