Pyruvate carboxylase deficiencies: complementation studies between "French" and "American" phenotypes in cultured fibroblasts.
Augereau, C
Pyruvate carboxylase deficiencies: complementation studies between "French" and "American" phenotypes in cultured fibroblasts. [electronic resource] - Journal of inherited metabolic disease 1985 - 59-62 p. digital
Publication Type: Comparative Study; Journal Article
0141-8955
10.1007/BF01801665 doi
Amino Acid Metabolism, Inborn Errors--genetics
Cells, Cultured
Fibroblasts--enzymology
Genetic Complementation Test
Humans
Multiple Carboxylase Deficiency--genetics
Mutation
Phenotype
Pyruvate Carboxylase--genetics
Pyruvate Carboxylase Deficiency Disease
Pyruvate carboxylase deficiencies: complementation studies between "French" and "American" phenotypes in cultured fibroblasts. [electronic resource] - Journal of inherited metabolic disease 1985 - 59-62 p. digital
Publication Type: Comparative Study; Journal Article
0141-8955
10.1007/BF01801665 doi
Amino Acid Metabolism, Inborn Errors--genetics
Cells, Cultured
Fibroblasts--enzymology
Genetic Complementation Test
Humans
Multiple Carboxylase Deficiency--genetics
Mutation
Phenotype
Pyruvate Carboxylase--genetics
Pyruvate Carboxylase Deficiency Disease