Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation

Lignende værker

• Mutations in the MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss
  af: Shearer, A. Eliot, et al.
  Udgivet: (2009)
• A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family
  af: Shearer, A. Eliot, et al.
  Udgivet: (2009)
• Mutations in TMC1 are a common cause of DFNB7/11 hearing loss in the Iranian population
  af: Hildebrand, Michael S., et al.
  Udgivet: (2010)
• When transcripts matter: delineating between non-syndromic hearing loss DFNB32 and hearing impairment infertile male syndrome (HIIMS)
  af: Mohseni, Marzieh, et al.
  Udgivet: (2020)
• Mutations in LOXHD1, an Evolutionarily Conserved Stereociliary Protein, Disrupt Hair Cell Function in Mice and Cause Progressive Hearing Loss in Humans
  af: Grillet, Nicolas, et al.
  Udgivet: (2009)