Contribution of CYP1B1 mutations and founder effect to primary congenital glaucoma in Mexico

Journal of Glaucoma

Volumn 17, Issue 3, 2008, Pages 189-192

  Zenteno, Juan Carlos ^a   Hernandez Merino, Elena ^a   Mejia Lopez, Herlinda ^a   Matías Florentino, Margarita ^a   Michel, Norma ^a   Elizondo Olascoaga, Celia ^b   Korder Ortega, Vincent ^b   Casab Rueda, Homero ^b   Garcia Ortiz, Jose Elias ^c  

^a INSTITUTE OF OPHTHALMOLOGY CONDE DE VALENCIANA   (Mexico)

^b Department of Glaucoma   (Mexico)

^c Western Biomedical Research Center   (Mexico)

Author keywords

Congenital glaucoma; CYP1B1; Founder mutation effect; Genetic heterogeneity

Indexed keywords

CYTOCHROME P450 1B1; DNA; GLUTAMIC ACID; LYSINE;

AMINO ACID SUBSTITUTION; ARTICLE; CLINICAL ARTICLE; COMPUTER PREDICTION; CONGENITAL GLAUCOMA; CONTROLLED STUDY; CYP1B1 GENE; DELETION MUTANT; DISEASE PREDISPOSITION; FOUNDER EFFECT; GENE; GENE FREQUENCY; GENE IDENTIFICATION; GENE MUTATION; GENETIC TRAIT; GLAUCOMA; HAPLOTYPE; HOMOZYGOSITY; HUMAN; HUMAN CELL; HUMAN TISSUE; INCIDENCE; INDONESIA; JAPANESE; MEXICO; MOLECULAR BIOLOGY; PATHOGENESIS; POPULATION RISK; PRIORITY JOURNAL; SAUDI ARABIA; SINGLE NUCLEOTIDE POLYMORPHISM; SLOVAKIA;

ADOLESCENT; ADULT; AMERICAN NATIVE CONTINENTAL ANCESTRY GROUP; CHILD; CHILD, PRESCHOOL; CONSANGUINITY; CYTOCHROME P-450 ENZYME SYSTEM; DNA MUTATIONAL ANALYSIS; FEMALE; FOUNDER EFFECT; GLAUCOMA; HUMANS; INFANT; MALE; MEXICO; MIDDLE AGED; MUTATION; POLYMERASE CHAIN REACTION;

EID: 42149113372     PISSN: 10570829     EISSN: None     Source Type: Journal    
DOI: 10.1097/IJG.0b013e31815678c3     Document Type: Article

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