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

Παρόμοια τεκμήρια

• 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
  ανά: Singh, Pawan Kumar, κ.ά.
  Έκδοση: (2017)
• Spectrum of GJB2 gene variants in Indian children with non-syndromic hearing loss
  ανά: Pawan Kumar Singh, κ.ά.
  Έκδοση: (2018-01-01)
• Spectrum of GJB2 gene variants in Indian children with non-syndromic hearing loss
  ανά: Singh, Pawan Kumar, κ.ά.
  Έκδοση: (2018)
• Frequency of primary mutations of Leber's hereditary optic neuropathy patients in North Indian population
  ανά: Mishra, Anushree, κ.ά.
  Έκδοση: (2017)
• The mutation spectrum in Indian patients with Gaucher disease
  ανά: Bisariya, Vartika, κ.ά.
  Έκδοση: (2011)