Auditory Neuropathy Spectrum Disorder due to Two Novel Compound Heterozygous OTOF Mutations in Two Chinese Families

Ítems similars

• Novel compound heterozygous mutations in the OTOF Gene identified by whole-exome sequencing in auditory neuropathy spectrum disorder
  per: Tang, Fengzhu, et al.
  Publicat: (2017)
• Variants of OTOF and PJVK Genes in Chinese Patients with Auditory Neuropathy Spectrum Disorder
  per: Jian, Wang, et al.
  Publicat: (2011)
• An OTOF Frameshift Variant Associated with Auditory Neuropathy Spectrum Disorder
  per: Xia, Hong, 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)
• Jervell and Lange-Nielsen Syndrome due to a Novel Compound Heterozygous KCNQ1 Mutation in a Chinese Family
  per: Qiu, Yue, et al.
  Publicat: (2020)