Ethnicity and mutations in GJB2 (connexin 26) and GJB6 (connexin 30) in a multi-cultural Canadian paediatric Cochlear Implant Program

This publication has 52 references indexed in Scilit:

• A genotype-phenotype correlation for GJB2 (connexin 26) deafness
  Journal of Medical Genetics, 2004
• Connexin 26 mutations in cases of sensorineural deafness in eastern Austria
  European Journal of Human Genetics, 2002
• Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations – phenotypic spectrum and frequencies of GJB2 mutations in Austria
  Human Genetics, 2002
• A Deletion Involving the Connexin 30 Gene in Nonsyndromic Hearing Impairment
  New England Journal of Medicine, 2002
• Temporal Bone Histopathology in Connexin 26–Related Hearing Loss
  The Laryngoscope, 2000
• Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene
  Human Molecular Genetics, 1997
• Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
  Nature, 1997
• Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis
  Brain Structure and Function, 1995
• Hearing Loss
  New England Journal of Medicine, 1993
• Potassium-induced release of an endogenous toxic activity for outer hair cells and auditory neurons in the cochlea: A new pathophysiological mechanism in Meniere's disease?
  Hearing Research, 1990