Genetic complementation in heterokaryons of human fibroblasts defective in cobalamin metabolism.

Inherited methylmalonicacidemia due to deficiency of methylmalonyl-CoA mutase (methylmalonyl-CoA CoA-carbonylmutase; EC 5.4.99.2) activity results from at least three classes of biochemically distinct defects affecting cobalamin (Cbl: vitamin B12) metabolism (cbl A, cbl B, and cbl C mutants) and a f...

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Autors principals: Gravel, R A, Mahoney, M J, Ruddle, F H, Rosenberg, L E
Format: Artigo
Idioma:Inglês
Publicat: 1975
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC432945/
https://ncbi.nlm.nih.gov/pubmed/1059104
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