DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3

Lignende værker

• Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79
  af: Rehman, Atteeq Ur, et al.
  Udgivet: (2010)
• DFNB86, a novel autosomal recessive nonsyndromic deafness locus on chromosome 16p13.3
  af: Ali, Rana A., et al.
  Udgivet: (2011)
• Molecular Basis of DFNB73: Mutations of BSND Can Cause Nonsyndromic Deafness or Bartter Syndrome
  af: Riazuddin, Saima, et al.
  Udgivet: (2009)
• Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome
  af: Ahmed, Zubair M., et al.
  Udgivet: (2008)
• Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p
  af: Rehman, Atteeq U., et al.
  Udgivet: (2011)