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Volumn 21, Issue 4, 2003, Pages 399-400
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Mutational spectrum in German patients with phenylalanine hydroxylase deficiency.
a
a
OLGAHOSPITAL
(Germany)
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Author keywords
[No Author keywords available]
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Indexed keywords
PHENYLALANINE 4 MONOOXYGENASE;
ARTICLE;
ETHNOLOGY;
FEMALE;
GENE FREQUENCY;
GENETIC SCREENING;
GENETICS;
GERMANY;
HETEROZYGOTE DETECTION;
HUMAN;
MALE;
NUCLEOTIDE SEQUENCE;
POPULATION GENETICS;
TURKEY (REPUBLIC);
DNA MUTATIONAL ANALYSIS;
FEMALE;
GENE FREQUENCY;
GENETIC SCREENING;
GENETICS, POPULATION;
GERMANY;
HETEROZYGOTE DETECTION;
HUMANS;
MALE;
PHENYLALANINE HYDROXYLASE;
TURKEY;
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EID: 0037389132
PISSN: None
EISSN: 10981004
Source Type: Journal
DOI: 10.1002/humu.9116 Document Type: Article |
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Times cited : (37)
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References (0)
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