Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene

Ítems similars

• OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele
  per: Varga, R, et al.
  Publicat: (2006)
• Q829X, a novel mutation in the gene encoding otoferlin (OTOF), is frequently found in Spanish patients with prelingual non-syndromic hearing loss
  per: Migliosi, V, et al.
  Publicat: (2002)
• Screening mutations of OTOF gene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathy
  per: Wang, Da-Yong, et al.
  Publicat: (2010)
• Elongated EABR wave latencies observed in patients with auditory neuropathy caused by OTOF mutation
  per: Hosoya, Makoto, et al.
  Publicat: (2018)
• A Novel Otoferlin Splice-Site Mutation in Siblings with Auditory Neuropathy Spectrum Disorder
  per: Runge, Christina L., et al.
  Publicat: (2013)