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Volumn 25, Issue 2, 2003, Pages 142-144
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Ten novel mutations in the phenylalanine hydroxylase gene identified in Chinese patients with phenylketonuria
a a a a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
PHENYLALANINE 4 MONOOXYGENASE;
ADULT;
ARTICLE;
CHILD;
DNA SEQUENCE;
ENZYMOLOGY;
EXON;
FEMALE;
GENETIC HETEROGENEITY;
GENETICS;
HUMAN;
INFANT;
MALE;
MISSENSE MUTATION;
MUTATION;
PHENYLKETONURIA;
ADULT;
CHILD;
EXONS;
FEMALE;
GENETIC HETEROGENEITY;
HUMANS;
INFANT;
MALE;
MUTATION;
MUTATION, MISSENSE;
PHENYLALANINE HYDROXYLASE;
PHENYLKETONURIAS;
SEQUENCE ANALYSIS, DNA;
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EID: 3042821262
PISSN: 1000503X
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (8)
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References (0)
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