In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment

Benzer Materyaller

• A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26)
  Yazar:: van Wijk, E, ve diğerleri
  Baskı/Yayın Bilgisi: (2003)
• DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23
  Yazar:: Moreno-Pelayo, M, ve diğerleri
  Baskı/Yayın Bilgisi: (2003)
• A Mutation in CCDC50, a Gene Encoding an Effector of Epidermal Growth Factor–Mediated Cell Signaling, Causes Progressive Hearing Loss
  Yazar:: Modamio-Høybjør, Silvia , ve diğerleri
  Baskı/Yayın Bilgisi: (2007)
• A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA50, maps to chromosome 7q32 between the DFNB17 and DFNB13 deafness loci
  Yazar:: Modamio-Hoybjor, S, ve diğerleri
  Baskı/Yayın Bilgisi: (2004)
• Mutations in the γ-Actin Gene (ACTG1) Are Associated with Dominant Progressive Deafness (DFNA20/26)
  Yazar:: Zhu, M., ve diğerleri
  Baskı/Yayın Bilgisi: (2003)