Cytochrome P450 1B1 gene mutations in Japanese patients with primary congenital glaucoma

American Journal of Ophthalmology

Volumn 131, Issue 3, 2001, Pages 345-350

  Kakiuchi Matsumoto, Tomoko ^a   Isashiki, Yasushi ^a   Ohba, Norio ^a   Kimura, Katsuaki ^a   Sonoda, Shozo ^a   Unoki, Kazuhiko ^a  

^a KAGOSHIMA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME P450 1B1;

ALLELE; AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CHILD; CLINICAL ARTICLE; CODON; CONGENITAL GLAUCOMA; CONTROLLED STUDY; DNA DETERMINATION; DNA SEQUENCE; FEMALE; GENE AMPLIFICATION; GENE MUTATION; GENETIC POLYMORPHISM; HUMAN; INFANT; JAPAN; LEUKOCYTE; MALE; MISSENSE MUTATION; PRIORITY JOURNAL;

AGE OF ONSET; ARYL HYDROCARBON HYDROXYLASES; CHILD; CHILD, PRESCHOOL; CYTOCHROME P-450 ENZYME SYSTEM; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; FEMALE; GLAUCOMA; HUMANS; INFANT; INFANT, NEWBORN; JAPAN; MALE; MUTATION, MISSENSE; PEDIGREE; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC;

EID: 0035123212     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9394(00)00808-4     Document Type: Article

References (13)

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