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Volumn 9, Issue , 2008, Pages
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C4B null alleles are not associated with genetic polymorphisms in the adjacent gene CYP21A2 in autism
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Author keywords
[No Author keywords available]
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Indexed keywords
COMPLEMENT COMPONENT C4B;
CYTOCHROME P450 21 A2;
STEROID 21 MONOOXYGENASE;
UNCLASSIFIED DRUG;
ARTICLE;
AUTISM;
CONTROLLED STUDY;
ENZYME INHIBITION;
FEMALE;
GENE EXPRESSION;
GENE FUNCTION;
GENE LOCUS;
GENE MUTATION;
GENETIC POLYMORPHISM;
GENOTYPE;
HUMAN;
HUMAN CELL;
MAJOR CLINICAL STUDY;
MALE;
POLYMERASE CHAIN REACTION;
PROTEIN DETERMINATION;
PROTEIN FUNCTION;
ALLELE;
CASE CONTROL STUDY;
ENZYMOLOGY;
GENE DELETION;
GENETIC LINKAGE;
GENETIC PREDISPOSITION;
GENETICS;
ALLELES;
AUTISTIC DISORDER;
CASE-CONTROL STUDIES;
COMPLEMENT C4B;
FEMALE;
GENETIC PREDISPOSITION TO DISEASE;
GENOTYPE;
HUMANS;
LINKAGE (GENETICS);
MALE;
POLYMORPHISM, GENETIC;
SEQUENCE DELETION;
STEROID 21-HYDROXYLASE;
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EID: 40549109279
PISSN: None
EISSN: 14712350
Source Type: Journal
DOI: 10.1186/1471-2350-9-1 Document Type: Article |
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Times cited : (10)
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References (28)
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