Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant. [electronic resource]
Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant. [electronic resource] — المؤلف: Willard, H F — Jan 1978
- المؤلف
- Willard, H F
- النشر
- Jan 1978
- الوصف
- 1-13 p.
- الموضوعات
- Cell Line؛ Genes, Recessive؛ Genetic Complementation Test؛ Humans؛ Isomerases؛ Methylmalonyl-CoA Mutase؛ Skin؛ Vitamin B 12 Deficiency