DFNB86, a novel autosomal recessive nonsyndromic deafness locus on chromosome 16p13.3

Ítems similars

• Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37
  per: Ahmed, Zubair M., et al.
  Publicat: (2003)
• DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3
  per: Khan, Shahid Yar, et al.
  Publicat: (2010)
• Molecular Basis of DFNB73: Mutations of BSND Can Cause Nonsyndromic Deafness or Bartter Syndrome
  per: Riazuddin, Saima, et al.
  Publicat: (2009)
• Mutations in TBC1D24, a Gene Associated With Epilepsy, Also Cause Nonsyndromic Deafness DFNB86
  per: Rehman, Atteeq U., et al.
  Publicat: (2014)
• Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome
  per: Ahmed, Zubair M., et al.
  Publicat: (2008)