TMC1 may be a common gene for nonsyndromic hereditary hearing loss in Indian population

Benzer Materyaller

• Identification of a novel homozygous mutation in transmembrane channel like 1 (TMC1) gene, one of the second-tier hearing loss genes after GJB2 in India
  Yazar:: Singh, Pawan Kumar, ve diğerleri
  Baskı/Yayın Bilgisi: (2017)
• Spectrum of GJB2 gene variants in Indian children with non-syndromic hearing loss
  Yazar:: Pawan Kumar Singh, ve diğerleri
  Baskı/Yayın Bilgisi: (2018-01-01)
• Spectrum of GJB2 gene variants in Indian children with non-syndromic hearing loss
  Yazar:: Singh, Pawan Kumar, ve diğerleri
  Baskı/Yayın Bilgisi: (2018)
• Frequency of primary mutations of Leber's hereditary optic neuropathy patients in North Indian population
  Yazar:: Mishra, Anushree, ve diğerleri
  Baskı/Yayın Bilgisi: (2017)
• The mutation spectrum in Indian patients with Gaucher disease
  Yazar:: Bisariya, Vartika, ve diğerleri
  Baskı/Yayın Bilgisi: (2011)