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A PvuII RFLP for the human liver arginase (ARG1) gene

✍ Scribed by Kidd, J.R.; Dizikes, G.J.; Grody, W.W.; Cederbaum, S.D.; Kidd, K.K.

Book ID
121460664
Publisher
Oxford University Press
Year
1986
Tongue
English
Weight
38 KB
Volume
14
Category
Article
ISSN
0305-1048

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Argininemia is a rare autossomal recessive disorder caused by deficiency in the cytosolic liver-type arginase enzyme (L-arginine urea-hydrolase; E.C. 3.5.3.1). In order to investigate the molecular basis for argininemia in four unrelated Portuguese patients (two from northern Portugal and two from M