Identification of novel mutations in glucocerebrosidase (GBA) gene in Indian patients with gaucher disease (GD)

Lignende værker

• Frequency analysis of Spinocerebellar ataxia types 1, 2, 3 & 6 in patients with ataxia from Gujarat
  af: Patel, Harsh, et al.
  Udgivet: (2014)
• Prenatal diagnosis of Tay-Sachs disease: our institutional experience
  af: Sheth, Jayesh, et al.
  Udgivet: (2014)
• Prenatal diagnosis of autosomal recessive osteopetrosis: a case report
  af: Mistri, Mehul, et al.
  Udgivet: (2014)
• Identification of novel mutations in HEXA gene in children affected with Tay-Sachs disease from India
  af: Mistri, Mehul, et al.
  Udgivet: (2014)
• Expanding the spectrum of HEXA mutations in Indian patients with Tay–Sachs disease
  af: Sheth, Jayesh, et al.
  Udgivet: (2014)