Pseudodominant inheritance of DFNB1 deafness due to the common 35delG mutation

Clin Genet. 2000 Mar;57(3):232-4. doi: 10.1034/j.1399-0004.2000.570311.x.
No abstract available

Publication types

  • Letter

MeSH terms

  • Alleles
  • Connexin 26
  • Connexins / genetics*
  • Family Health
  • Female
  • Gene Deletion*
  • Genes, Dominant*
  • Hearing Loss, Sensorineural / genetics*
  • Homozygote
  • Humans
  • Infant
  • Male
  • Pedigree
  • Polymerase Chain Reaction

Substances

  • Connexins
  • GJB2 protein, human
  • Connexin 26