Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss

Antzeko izenburuak

• Screening of 10 DFNB Loci Causing Autosomal Recessive Non-Syndromic Hearing Loss in Two Iranian Populations Negative for GJB2 Mutations
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  Argitaratua: (2019)
• Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran
  nork: ASGHARZADE, Samira, et al.
  Argitaratua: (2017)
• Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked family
  nork: Reiisi, Somayeh, et al.
  Argitaratua: (2016)
• Investigation of LRTOMT gene (locus DFNB63) mutations in Iranian patients with autosomal recessive non-syndromic hearing loss
  nork: Taghizadeh, Seyyed Hossein, et al.
  Argitaratua: (2013)
• Genetic Linkage Analysis of the DFNB21 Locus in Autosomal Recessive Hearing Loss in Large Families from Khuzestan Province
  nork: Mahtab Khosrofar, et al.
  Argitaratua: (2017-06-01)