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Volumn 21, Issue 3, 2000, Pages 191-193
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Novel compound hoterozygous mutations in the cytochrome P4501B1 gene (CYP1B1) in a Japanese patient with primary congenital glaucoma
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Author keywords
Congenital glaucoma; CYP1B1; Cytochrome P4501B1; Mutation
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Indexed keywords
CYTOCHROME P450;
CYTOCHROME P450 1B1;
UNCLASSIFIED DRUG;
CYTOCHROME P 450 CYP1B1;
CYTOCHROME P-450 CYP1B1;
PRIMER DNA;
UNSPECIFIC MONOOXYGENASE;
ADOLESCENT;
ADULT;
ARTICLE;
CASE REPORT;
CHILD;
CONGENITAL GLAUCOMA;
DIAGNOSTIC VALUE;
FEMALE;
GENE AMPLIFICATION;
GENE LOCUS;
HETEROZYGOSITY;
HUMAN;
HUMAN CELL;
HUMAN TISSUE;
JAPAN;
MALE;
POLYMERASE CHAIN REACTION;
PRIORITY JOURNAL;
CHEMISTRY;
DNA SEQUENCE;
ETHNOLOGY;
GENETICS;
GLAUCOMA;
INFANT;
MUTATION;
NUCLEOTIDE SEQUENCE;
PEDIGREE;
PRESCHOOL CHILD;
ADOLESCENT;
ADULT;
ARYL HYDROCARBON HYDROXYLASES;
BASE SEQUENCE;
CHILD;
CHILD, PRESCHOOL;
CYTOCHROME P-450 ENZYME SYSTEM;
DNA MUTATIONAL ANALYSIS;
DNA PRIMERS;
FEMALE;
GLAUCOMA;
HUMANS;
INFANT;
MALE;
MUTATION;
PEDIGREE;
POLYMERASE CHAIN REACTION;
SEQUENCE ANALYSIS, DNA;
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EID: 0033623590
PISSN: 13816810
EISSN: None
Source Type: Journal
DOI: 10.1076/1381-6810(200009)21:3;1-z;ft191 Document Type: Article |
Times cited : (18)
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References (9)
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