A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3.

Podobne zapisy

• A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA13, maps to chromosome 6p.
  od: Brown, M R, i wsp.
  Wydane: (1997)
• A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus
  od: Van Camp, G., i wsp.
  Wydane: (1999)
• A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.
  od: Verhoeven, K, i wsp.
  Wydane: (1997)
• Exome Sequencing Identifies a Novel CEACAM16 Mutation Associated with Autosomal Dominant Nonsyndromic Hearing Loss DFNA4B in a Chinese Family
  od: Wang, Honghan, i wsp.
  Wydane: (2015)
• A novel locus (DFNA23) for prelingual autosomal dominant nonsyndromic hearing loss maps to 14q21-q22 in a Swiss German kindred.
  od: Salam, A A, i wsp.
  Wydane: (2000)