Frequency analysis of Spinocerebellar ataxia types 1, 2, 3 & 6 in patients with ataxia from Gujarat

Samankaltaisia teoksia

• Prenatal diagnosis of autosomal recessive osteopetrosis: a case report
  Tekijä: Mistri, Mehul, et al.
  Julkaistu: (2014)
• Autosomal dominant mutation in COL7A1 gene causing epidermolysis bullosa dystrophica
  Tekijä: Sheth, Jayesh, et al.
  Julkaistu: (2014)
• Identification of novel mutations in glucocerebrosidase (GBA) gene in Indian patients with gaucher disease (GD)
  Tekijä: Ankleshwaria, Chitra, et al.
  Julkaistu: (2014)
• Frequency of Spinocerebellar Ataxia type 1, 2, 3,6 and 7 and clinical profile of Spinocerebellar Ataxia type 3 in Malaysia
  Tekijä: Mohamed Ibrahim, Norlinah, et al.
  Julkaistu: (2020)
• Biochemical and molecular characterization of adult patients with type I Gaucher disease and carrier frequency analysis of Leu444Pro - a common Gaucher disease mutation in India
  Tekijä: Sheth, Jayesh, et al.
  Julkaistu: (2018)