Clue to a New Deafness Gene: A Large Chinese Nonsyndromic Hearing Loss Family Linked to DFNA4

Ítems similars

• A mouse model for nonsyndromic deafness (DFNB12) links hearing loss to defects in tip links of mechanosensory hair cells
  per: Schwander, Martin, et al.
  Publicat: (2009)
• A Novel DFNA36 Mutation in TMC1 Orthologous to the Beethoven (Bth) Mouse Associated with Autosomal Dominant Hearing Loss in a Chinese Family
  per: Zhao, Yali, et al.
  Publicat: (2014)
• Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss
  per: Atik, Tahir, et al.
  Publicat: (2015)
• A POU3F4 Mutation Causes Nonsyndromic Hearing Loss in a Chinese X-linked Recessive Family
  per: Du, Wan, et al.
  Publicat: (2017)
• A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA13, maps to chromosome 6p.
  per: Brown, M R, et al.
  Publicat: (1997)