A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3

Những quyển sách tương tự

• A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus
  Bằng: Van Camp, G., et al.
  Được phát hành: (1999)
• A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA13, maps to chromosome 6p.
  Bằng: Brown, M R, et al.
  Được phát hành: (1997)
• A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26)
  Bằng: van Wijk, E, et al.
  Được phát hành: (2003)
• Mapping of a new autosomal dominant non-syndromic hearing loss locus (DFNA43) to chromosome 2p12
  Bằng: Flex, E, et al.
  Được phát hành: (2003)
• DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23
  Bằng: Moreno-Pelayo, M, et al.
  Được phát hành: (2003)