(Q28024608)
English
autosomal recessive nonsyndromic deafness 25
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with moderate to profound, progressive hearing loss and has material basis in mutation in the GRXCR1 gene on chromosome 4p13
- DFNB25
- autosomal recessive deafness 25
- DEAFNESS, AUTOSOMAL RECESSIVE 25; DFNB25
- DEAFNESS, AUTOSOMAL RECESSIVE 25
- Deafness, Autosomal Recessive type 25
- autosomal recessive nonsyndromic deafness type 25
Statements
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Identifiers
1 reference
2 references
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1 reference