Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families

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• Corrigendum to “Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families”
  gan: Bai, Xiaohui, et al.
  Cyhoeddwyd: (2020)
• Three MYO15A Mutations Identified in One Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss
  gan: Zhang, Fengguo, et al.
  Cyhoeddwyd: (2018)
• A novel MYH14 mutation in a Chinese family with autosomal dominant nonsyndromic hearing loss
  gan: Wang, Mingming, et al.
  Cyhoeddwyd: (2020)
• Identification of two novel mutations in POU4F3 gene associated with autosomal dominant hearing loss in Chinese families
  gan: Bai, Xiaohui, et al.
  Cyhoeddwyd: (2020)
• Identification of Novel Compound Heterozygous MYO15A Mutations in Two Chinese Families with Autosomal Recessive Nonsyndromic Hearing Loss
  gan: Wang, Xiao-Hui, et al.
  Cyhoeddwyd: (2021)