A locus for autosomal dominant keratoconus maps to human chromosome 3p14–q13

Míreanna Comhchosúla

• Autosomal dominant hereditary benign telangiectasia maps to the CMC1 locus for capillary malformation on chromosome 5q14
  le: Brancati, F, et al.
  Foilsithe: (2003)
• A novel locus for autosomal dominant non‐syndromic deafness, DFNA53, maps to chromosome 14q11.2‐q12
  le: Yan, D, et al.
  Foilsithe: (2006)
• A gene responsible for autosomal dominant auditory neuropathy (AUNA1) maps to 13q14–21
  le: Kim, T, et al.
  Foilsithe: (2004)
• Mapping of a new autosomal dominant non-syndromic hearing loss locus (DFNA43) to chromosome 2p12
  le: Flex, E, et al.
  Foilsithe: (2003)
• A Locus for Autosomal Dominant “Pure” Hereditary Spastic Paraplegia Maps to Chromosome 19q13
  le: Reid, E., et al.
  Foilsithe: (2000)