Screening for MYO15A Gene Mutations in Autosomal Recessive Nonsyndromic, GJB2 Negative Iranian Deaf Population

Podobne zapisy

• Did the GJB2 35delG Mutation Originate in Iran?
  od: Norouzi, Vahideh, i wsp.
  Wydane: (2011)
• Prevalence Study of GJB2 Gene Mutations in Iranian Ethnics
  od: Kimia Kahrizi, i wsp.
  Wydane: (2007-10-01)
• When transcripts matter: delineating between non-syndromic hearing loss DFNB32 and hearing impairment infertile male syndrome (HIIMS)
  od: Mohseni, Marzieh, i wsp.
  Wydane: (2020)
• Two Iranian Families with a Novel Mutation in GJB2 Causing Autosomal Dominant Nonsyndromic Hearing Loss
  od: Bazazzadegan, Niloofar, i wsp.
  Wydane: (2011)
• Spectrum of Gjb2 Gene Mutations in Nonsyndromic Autosomal Recessive Deaf Patients in Yazd
  od: H Najmabadi, i wsp.
  Wydane: (2005-10-01)