Mutations in TMC1 are a common cause of DFNB7/11 hearing loss in the Iranian population

Podobné jednotky

• Screening for MYO15A Gene Mutations in Autosomal Recessive Nonsyndromic, GJB2 Negative Iranian Deaf Population
  Autor: Fattahi, Zohreh, a další
  Vydáno: (2012)
• A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family
  Autor: Shearer, A. Eliot, a další
  Vydáno: (2009)
• Mutations in the MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss
  Autor: Shearer, A. Eliot, a další
  Vydáno: (2009)
• Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation
  Autor: Hildebrand, Michael S., a další
  Vydáno: (2010)
• Investigating Seven Recently Identified Genes in 100 Iranian Families with Autosomal Recessive Non-syndromic Hearing Loss
  Autor: Reihaneh Alikhani, a další
  Vydáno: (2015-09-01)