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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".

Xiaohui BaiChi ZhangFengguo ZhangYun XiaoYu JinHai-Bo WangLei Xu
Published in: BioMed research international (2020)
[This corrects the article DOI: 10.1155/2020/1685974.].
Keyphrases
  • hearing loss
  • copy number
  • intellectual disability
  • genome wide
  • genome wide identification
  • muscular dystrophy
  • gene expression
  • autism spectrum disorder
  • genome wide analysis
  • duchenne muscular dystrophy