Prevalent connexin 26 gene (GJB2) mutations in Japanese

Eitemau Tebyg

• Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss.
  gan: Kelley, P M, et al.
  Cyhoeddwyd: (1998)
• Recurrent mutations in the deafness gene GJB2 (connexin 26) in British Asian families
  gan: Rickard, S., et al.
  Cyhoeddwyd: (2001)
• Absence of mutations in GJB2 (Connexin-26) gene in an ethnic group of southwest Iran
  gan: Galehdari, Hamid, et al.
  Cyhoeddwyd: (2009)
• A novel C202F mutation in the connexin26 gene (GJB2) associated with autosomal dominant isolated hearing loss
  gan: Morle, L., et al.
  Cyhoeddwyd: (2000)
• Evaluation of electrocardiographic parameters in patients with hearing loss genotyped for the connexin 26 gene (GJB2) mutations
  gan: Agnieszka Sanecka, et al.
  Cyhoeddwyd: (2017)