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Volumn 14, Issue 4, 1999, Pages 355-356
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Identification of a novel R21X mutation in the liver-type arginase gene (ARG1) in four Portuguese patients with argininemia.
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Author keywords
[No Author keywords available]
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Indexed keywords
ARGINASE;
ARGININE;
ARTICLE;
BLOOD;
CHILD;
CHROMOSOME 6;
DISORDERS OF AMINO ACID AND PROTEIN METABOLISM;
FEMALE;
GENETICS;
HUMAN;
MALE;
NUCLEOTIDE SEQUENCE;
POINT MUTATION;
POLYMERASE CHAIN REACTION;
PRESCHOOL CHILD;
AMINO ACID METABOLISM, INBORN ERRORS;
ARGINASE;
ARGININE;
BASE SEQUENCE;
CHILD;
CHILD, PRESCHOOL;
CHROMOSOMES, HUMAN, PAIR 6;
FEMALE;
HUMANS;
MALE;
POINT MUTATION;
POLYMERASE CHAIN REACTION;
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EID: 0033208662
PISSN: None
EISSN: 10981004
Source Type: Journal
DOI: 10.1002/(SICI)1098-1004(199910)14:4<355::AID-HUMU20>3.0.CO;2-I Document Type: Article |
Times cited : (18)
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References (0)
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