GJB2 Mutations in Mongolia: Complex Alleles, Low Frequency, and Reduced Fitness of the Deaf

Lignende værker

• Heterogenous Point Mutations in the Mitochondrial tRNA Ser(UCN) Precursor Coexisting with the A1555G Mutation in Deaf Students from Mongolia
  af: Pandya, Arti, et al.
  Udgivet: (1999)
• Analyses of del(GJB6‐D13S1830) and del(GJB6‐D13S1834) deletions in a large cohort with hearing loss: Caveats to interpretation of molecular test results in multiplex families
  af: Pandya, Arti, et al.
  Udgivet: (2020)
• Molecular epidemiology of Chinese Han deaf patients with bi-allelic and mono-allelic GJB2 mutations
  af: Yu, Xiaoyu, et al.
  Udgivet: (2020)
• Fitness among individuals with early childhood deafness: studies in alumni families from Gallaudet University
  af: BLANTON, SUSAN H., et al.
  Udgivet: (2009)
• Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity.
  af: Pandya, A, et al.
  Udgivet: (1997)