Sequence of DNA flanking the exons of the HEXA gene, and identification of mutations in Tay-Sachs disease.

Lignende værker

• Diagnostic heteroduplexes: simple detection of carriers of a 4-bp insertion mutation in Tay-Sachs disease.
  af: Triggs-Raine, B L, et al.
  Udgivet: (1990)
• Mutational analyses of Tay-Sachs disease: studies on Tay-Sachs carriers of French Canadian background living in New England.
  af: Triggs-Raine, B, et al.
  Udgivet: (1995)
• Novel mutations and DNA-based screening in non-Jewish carriers of Tay-Sachs disease.
  af: Akerman, B R, et al.
  Udgivet: (1997)
• Identification of Novel Mutations in HEXA Gene in Children Affected with Tay Sachs Disease from India
  af: Mistri, Mehul, et al.
  Udgivet: (2012)
• Identification of novel mutations in HEXA gene in children affected with Tay-Sachs disease from India
  af: Mistri, Mehul, et al.
  Udgivet: (2014)