Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction

This publication has 26 references indexed in Scilit:

• Association of Unconventional Myosin MYO15 Mutations with Human Nonsyndromic Deafness DFNB3
  Science, 1998
• Connexin 26 gene linked to a dominant deafness
  Nature, 1998
• Novel Mutations in the Connexin 26 Gene (GJB2) That Cause Autosomal Recessive (DFNB1) Hearing Loss
  American Journal of Human Genetics, 1998
• Connexin mutations and hearing loss
  Nature, 1998
• Nonsyndromic Deafness DFNA1 Associated with Mutation of a Human Homolog of the Drosophila Gene diaphanous
  Science, 1997
• Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene
  Nature Genetics, 1997
• The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene
  Nature Genetics, 1997
• Mutations in the myosin VIIA gene cause non-syndromic recessive deafness
  Nature Genetics, 1997
• Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
  Nature, 1997
• Genes responsible for human hereditary deafness: symphony of a thousand
  Nature Genetics, 1996