Mutation Screening of Exons 7 and 13 of the TMC1 Gene in Autosomal Recessive Non-syndromic Hearing Loss (ARNSHL) in Iran

Lignende værker

• Investigation of LRTOMT gene (locus DFNB63) mutations in Iranian patients with autosomal recessive non-syndromic hearing loss
  af: Taghizadeh, Seyyed Hossein, et al.
  Udgivet: (2013)
• Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran
  af: ASGHARZADE, Samira, et al.
  Udgivet: (2017)
• A preliminary study of inherited thrombophilic risk factors in different clinical manifestations of venous thromboembolism in central Iran
  af: Karimi, Ali, et al.
  Udgivet: (2015)
• Investigation of Mutations in Exons 15 and 18 of MYBPC3 Gene in Hypertrophic Cardiomyopathy Patients
  af: Behnaz Sadat Abedi, et al.
  Udgivet: (2015-08-01)
• Screening of 10 DFNB Loci Causing Autosomal Recessive Non-Syndromic Hearing Loss in Two Iranian Populations Negative for GJB2 Mutations
  af: KOOHIYAN, Mahbobeh, et al.
  Udgivet: (2019)