Mutations in the MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss

Míreanna Comhchosúla

• Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation
  le: Hildebrand, Michael S., et al.
  Foilsithe: (2010)
• A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family
  le: Shearer, A. Eliot, et al.
  Foilsithe: (2009)
• Mutations in TMC1 are a common cause of DFNB7/11 hearing loss in the Iranian population
  le: Hildebrand, Michael S., et al.
  Foilsithe: (2010)
• When transcripts matter: delineating between non-syndromic hearing loss DFNB32 and hearing impairment infertile male syndrome (HIIMS)
  le: Mohseni, Marzieh, et al.
  Foilsithe: (2020)
• Screening for MYO15A Gene Mutations in Autosomal Recessive Nonsyndromic, GJB2 Negative Iranian Deaf Population
  le: Fattahi, Zohreh, et al.
  Foilsithe: (2012)