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

Lignende værker

• Three MYO15A Mutations Identified in One Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss
  af: Zhang, Fengguo, et al.
  Udgivet: (2018)
• Identification of Novel Compound Heterozygous MYO15A Mutations in Two Chinese Families with Autosomal Recessive Nonsyndromic Hearing Loss
  af: Wang, Xiao-Hui, et al.
  Udgivet: (2021)
• Compound Heterozygous Mutations in TMC1 and MYO15A Are Associated with Autosomal Recessive Nonsyndromic Hearing Loss in Two Chinese Han Families
  af: Xu, Pengcheng, et al.
  Udgivet: (2020)
• GJB2 c.235delC variant associated with autosomal recessive nonsyndromic hearing loss and auditory neuropathy spectrum disorder
  af: Xia, Hong, et al.
  Udgivet: (2019)
• Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families
  af: Woo, Hae-Mi, et al.
  Udgivet: (2013)