A new locus for nonsyndromic hereditary hearing impairment, DFNA17, maps to chromosome 22 and represents a gene for cochleosaccular degeneration.

Eitemau Tebyg

• Human Nonsyndromic Hereditary Deafness DFNA17 Is Due to a Mutation in Nonmuscle Myosin MYH9
  gan: Lalwani, Anil K., et al.
  Cyhoeddwyd: (2000)
• DFNA25, a Novel Locus for Dominant Nonsyndromic Hereditary Hearing Impairment, Maps to 12q21-24
  gan: Greene, Charles C., et al.
  Cyhoeddwyd: (2001)
• A novel locus (DFNA23) for prelingual autosomal dominant nonsyndromic hearing loss maps to 14q21-q22 in a Swiss German kindred.
  gan: Salam, A A, et al.
  Cyhoeddwyd: (2000)
• A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA13, maps to chromosome 6p.
  gan: Brown, M R, et al.
  Cyhoeddwyd: (1997)
• A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.
  gan: Verhoeven, K, et al.
  Cyhoeddwyd: (1997)