Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant.

Lignende værker

• Inherited Methylmalonyl CoA Mutase Apoenzyme Deficiency in Human Fibroblasts: EVIDENCE FOR ALLELIC HETEROGENEITY, GENETIC COMPOUNDS, AND CODOMINANT EXPRESSION
  af: Willard, Huntington F., et al.
  Udgivet: (1980)
• Delivery of tailor-made cobalamin to methylmalonyl-CoA mutase
  af: Bandarian, Vahe
  Udgivet: (2008)
• Recognition of two intracellular cobalamin binding proteins and their identification as methylmalonyl-CoA mutase and methionine synthetase.
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  Udgivet: (1977)
• Primary structure and activity of mouse methylmalonyl-CoA mutase.
  af: Wilkemeyer, M F, et al.
  Udgivet: (1990)
• Adenoviral-mediated correction of methylmalonyl-CoA mutase deficiency in murine fibroblasts and human hepatocytes
  af: Chandler, Randy J, et al.
  Udgivet: (2007)