Cloning and expression of mutations demonstrating intragenic complementation in mut0 methylmalonic aciduria.

Ítems similars

• Genetic characterization of a MUT locus mutation discriminating heterogeneity in mut0 and mut- methylmalonic aciduria by interallelic complementation.
  per: Raff, M L, et al.
  Publicat: (1991)
• Cloning and expression of a mutant methylmalonyl coenzyme A mutase with altered cobalamin affinity that causes mut- methylmalonic aciduria.
  per: Crane, A M, et al.
  Publicat: (1992)
• Differential diagnosis of mut and cbl methylmalonic aciduria by DNA-mediated gene transfer in primary fibroblasts.
  per: Wilkemeyer, M F, et al.
  Publicat: (1991)
• Heterozygous mutations at the mut locus in fibroblasts with mut0 methylmalonic acidemia identified by polymerase-chain-reaction cDNA cloning.
  per: Jansen, R, et al.
  Publicat: (1990)
• Clustering of mutations in methylmalonyl CoA mutase associated with mut- methylmalonic acidemia.
  per: Crane, A. M., et al.
  Publicat: (1994)