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

Similar Items

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