Newer trends in the genetic and biochemical studies in the etiopathogenesis of aminoacidopathies.

Nair, K R; Virmani, V

Nair, K R; Virmani, V.

Neurol India ; 1973 Sep; 21(3): 128-36

Article in English | IMSEAR | ID: sea-121063

Subject(s)

Amino Acid Metabolism, Inborn Errors/drug therapy; Amino Acids, Sulfur/metabolism; Base Sequence; Coenzymes/metabolism; DNA; Enzymes/biosynthesis; Genes, Regulator; Humans; Infant; Leucine/metabolism; Mutation; Pyridoxine/metabolism; Syndrome; Tryptophan/metabolism; Vitamin B 12/metabolism

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Pyridoxine / Syndrome / Tryptophan / Vitamin B 12 / Humans / DNA / Base Sequence / Genes, Regulator / Coenzymes / Enzymes Language: English Journal: Neurol India Year: 1973 Type: Article

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