(Q28024720)
English
autosomal dominant nonsyndromic deafness 69
autosomal dominant nonsyndromic deafness that has material basis in mutation in the KITLG gene on chromosome 12q21
- DCUA
- DFNA69
- autosomal dominant deafness 69
- unilateral or asymmetric congenital deafness
- Deafness, Congenital, Unilateral or Asymmetric
- autosomal dominant nonsyndromic deafness type 69
Statements
1 reference
1 reference
Identifiers
1 reference
2 references
1 reference
1 reference