Identification of Novel Compound Heterozygous MYO15A Mutations in Two Chinese Families with Autosomal Recessive Nonsyndromic Hearing Loss

Registos relacionados

• 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 em: (2020)
• Three MYO15A Mutations Identified in One Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss
  Por: Zhang, Fengguo, et al.
  Publicado em: (2018)
• Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss
  Por: Xia, Hong, et al.
  Publicado em: (2015)
• Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencing
  Por: Gao, Xue, et al.
  Publicado em: (2013)
• Autosomal Recessive Congenital Sensorineural Hearing Loss due to a Novel Compound Heterozygous PTPRQ Mutation in a Chinese Family
  Por: Wu, Xia, et al.
  Publicado em: (2018)