Identification of novel mutations in HEXA gene in children affected with Tay-Sachs disease from India

Samankaltaisia teoksia

• Identification of Novel Mutations in HEXA Gene in Children Affected with Tay Sachs Disease from India
  Tekijä: Mistri, Mehul, et al.
  Julkaistu: (2012)
• Expanding the spectrum of HEXA mutations in Indian patients with Tay–Sachs disease
  Tekijä: Sheth, Jayesh, et al.
  Julkaistu: (2014)
• Prenatal diagnosis of Tay-Sachs disease: our institutional experience
  Tekijä: Sheth, Jayesh, et al.
  Julkaistu: (2014)
• Identification of deletion-duplication in HEXA gene in five children with Tay-Sachs disease from India
  Tekijä: Sheth, Jayesh, et al.
  Julkaistu: (2018)
• Identification of novel mutations in glucocerebrosidase (GBA) gene in Indian patients with gaucher disease (GD)
  Tekijä: Ankleshwaria, Chitra, et al.
  Julkaistu: (2014)