Identification of novel compound heterozygous mutations of the MYO15A gene with autosomal recessive non‐syndromic hearing loss

Ejemplares similares

• Identification of Novel Compound Heterozygous MYO15A Mutations in Two Chinese Families with Autosomal Recessive Nonsyndromic Hearing Loss
  por: Wang, Xiao-Hui, et al.
  Publicado: (2021)
• Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencing
  por: Gao, Xue, et al.
  Publicado: (2013)
• Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss
  por: Bakhchane, Amina, et al.
  Publicado: (2017)
• Compound Heterozygous Mutations in TMC1 and MYO15A Are Associated with Autosomal Recessive Nonsyndromic Hearing Loss in Two Chinese Han Families
  por: Xu, Pengcheng, et al.
  Publicado: (2020)
• Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss
  por: Xia, Hong, et al.
  Publicado: (2015)