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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| Vydáno v: | Proc Natl Acad Sci U S A |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
National Academy of Sciences
1975
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC432945/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1059104/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.72.8.3181 |
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