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

Name: Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant.
Author: Willard, H F

Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant. — المؤلف: Willard, H F — American journal of human genetics Jan 1978

المؤلف: Willard, H F
النشر: American journal of human genetics Jan 1978
الوصف: 1-13 p.
الموضوعات: Cell Line؛ Genes, Recessive؛ Genetic Complementation Test؛ Humans؛ Isomerases؛ Methylmalonyl-CoA Mutase؛ Skin؛ Vitamin B 12 Deficiency