Molecular analysis of the CYP1B1 gene: Identification of novel truncating mutations in patients with primary congenital glaucoma

Ophthalmic Research

Volumn 39, Issue 1, 2007, Pages 17-23

  Messina Baas, O M ^a   Gonzalez Huerta L M ^a   Chima Galan C ^a   Kofman Alfaro, S H ^a   Rivera Vega, M R ^a   Babayan Mena I ^a   Cuevas Covarrubias, S A ^a  

^a HOSPITAL GENERAL DE MÉXICO   (Mexico)

Author keywords

CYP1B1 gene; Polymorphism; Primary congenital glaucoma

Indexed keywords

ALANINE; ARGININE; CYTOCHROME P450 1B1; DNA; LEUCINE; PROLINE;

ADOLESCENT; ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; CHILD; CODON; CONGENITAL GLAUCOMA; DIAGNOSTIC PROCEDURE; DNA SEQUENCE; FEMALE; GENE DELETION; GENE DUPLICATION; GENE IDENTIFICATION; GENE MUTATION; GENETIC ANALYSIS; GENETIC COUNSELING; GENETIC POLYMORPHISM; GENETIC VARIABILITY; GENOMICS; HUMAN; MALE; MOLECULAR BIOLOGY; MOLECULAR GENETICS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; STOP CODON;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CONSANGUINITY; CYTOCHROME P-450 ENZYME SYSTEM; DNA; DNA MUTATIONAL ANALYSIS; FEMALE; GLAUCOMA; HUMANS; MALE; MUTATION; PEDIGREE; POLYMORPHISM, GENETIC;

EID: 33846242906     PISSN: 00303747     EISSN: None     Source Type: Journal    
DOI: 10.1159/000097902     Document Type: Article

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