Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss

Ítems similars

• Three MYO15A Mutations Identified in One Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss
  per: Zhang, Fengguo, et al.
  Publicat: (2018)
• Identification of Novel Compound Heterozygous MYO15A Mutations in Two Chinese Families with Autosomal Recessive Nonsyndromic Hearing Loss
  per: Wang, Xiao-Hui, et al.
  Publicat: (2021)
• Identification of Novel Compound Heterozygous MYO15A Mutations in Two Chinese Families with Autosomal Recessive Nonsyndromic Hearing Loss
  per: Xiao-Hui Wang, et al.
  Publicat: (2021-01-01)
• Compound Heterozygous Mutations in TMC1 and MYO15A Are Associated with Autosomal Recessive Nonsyndromic Hearing Loss in Two Chinese Han Families
  per: Xu, Pengcheng, et al.
  Publicat: (2020)
• Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families
  per: Woo, Hae-Mi, et al.
  Publicat: (2013)