Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran

Documenti analoghi

• 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
  di: Reiisi, Somayeh, et al.
  Pubblicazione: (2016)
• Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees
  di: Khatami, Somayeh, et al.
  Pubblicazione: (2020)
• Screening of 10 DFNB Loci Causing Autosomal Recessive Non-Syndromic Hearing Loss in Two Iranian Populations Negative for GJB2 Mutations
  di: KOOHIYAN, Mahbobeh, et al.
  Pubblicazione: (2019)
• The Study of SLC26A4 Gene Causing Autosomal Recessive Hearing Loss by Linkage Analysis in a Cohort of Iranian Populations
  di: Reiisi, Somayeh, et al.
  Pubblicazione: (2014)
• Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss
  di: Tabatabaiefar, MA, et al.
  Pubblicazione: (2011)