Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness

Samankaltaisia teoksia

• Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction
  Tekijä: Naz, S, et al.
  Julkaistu: (2004)
• GJB2 Mutations in Mongolia: Complex Alleles, Low Frequency, and Reduced Fitness of the Deaf
  Tekijä: Tekin, Mustafa, et al.
  Julkaistu: (2010)
• Heterogenous Point Mutations in the Mitochondrial tRNA Ser(UCN) Precursor Coexisting with the A1555G Mutation in Deaf Students from Mongolia
  Tekijä: Pandya, Arti, et al.
  Julkaistu: (1999)
• SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities
  Tekijä: Pryor, S, et al.
  Julkaistu: (2005)
• Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness
  Tekijä: Ben-Yosef, T., et al.
  Julkaistu: (2001)