A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunction

Benzer Materyaller

• Hearing and vestibular deficits in the Coch(−/−) null mouse model: comparison to the Coch(G88E/G88E) mouse and to DFNA9 hearing and balance disorder
  Yazar:: Jones, Sherri M., ve diğerleri
  Baskı/Yayın Bilgisi: (2010)
• Cochlin in Normal Middle Ear and Abnormal Middle Ear Deposits in DFNA9 and Coch(G88E/G88E) Mice
  Yazar:: Robertson, Nahid G., ve diğerleri
  Baskı/Yayın Bilgisi: (2014)
• A Novel Mutation in COCH – Implications for Genotype-Phenotype Correlations in DFNA9 Hearing Loss
  Yazar:: Hildebrand, Michael S., ve diğerleri
  Baskı/Yayın Bilgisi: (2010)
• Identification of pathogenic mechanisms of COCH mutations, abolished cochlin secretion and intracellular aggregate formation: genotype-phenotype correlations in DFNA9 deafness and vestibular disorder
  Yazar:: Bae, Seung-Hyun, ve diğerleri
  Baskı/Yayın Bilgisi: (2014)
• Histopathology of the Human Inner Ear in the p.L114P COCH Mutation (DFNA9)
  Yazar:: Burgess, Barbara J., ve diğerleri
  Baskı/Yayın Bilgisi: (2016)