DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23

Lignende værker

• A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA50, maps to chromosome 7q32 between the DFNB17 and DFNB13 deafness loci
  af: Modamio-Hoybjor, S, et al.
  Udgivet: (2004)
• In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment
  af: Morín, Matías, et al.
  Udgivet: (2009)
• Q829X, a novel mutation in the gene encoding otoferlin (OTOF), is frequently found in Spanish patients with prelingual non-syndromic hearing loss
  af: Migliosi, V, et al.
  Udgivet: (2002)
• DFNA8/12 Caused by TECTA Mutations is the Most Identified Subtype of Non-syndromic Autosomal Dominant Hearing Loss
  af: Hildebrand, Michael S., et al.
  Udgivet: (2011)
• A novel locus for autosomal dominant non‐syndromic deafness, DFNA53, maps to chromosome 14q11.2‐q12
  af: Yan, D, et al.
  Udgivet: (2006)