Primary congenital glaucoma and Rieger's anomaly: Extended haplotypes reveal founder effects for eight distinct CYP1B1 mutations

Molecular Vision

Volumn 12, Issue , 2006, Pages 523-531

  Chavarria Soley, Gabriela ^a   Michels Rautenstrauss, Karin ^a   Pasutto, Francesca ^a   Flikier, David ^b   Flikier, Paul ^c   Cirak, Sebahattin ^d   Bejjani, Bassem ^e   Winters, Daniel L ^e   Lewis, Richard A ^f   Mardin, Christian ^a   Reis, Andre ^a   Rautenstrauss, Bernard ^a  

^a UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

^b Instituto de Cirugia Ocular   (Costa Rica)

^c Centro Medico de la Vision   (Costa Rica)

^d UNIVERSITY HOSPITAL ESSEN   (Germany)

^e WASHINGTON STATE UNIVERSITY   (United States)

^f BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME P450; CYTOCHROME P450 1B1; LIPID; MICROSATELLITE DNA; STEROID; UNSPECIFIC MONOOXYGENASE;

ARTICLE; CATALYSIS; CHEMICAL REACTION; CLINICAL ARTICLE; CONGENITAL GLAUCOMA; CONTROLLED STUDY; DRUG METABOLISM; ETHNIC GROUP; FOUNDER EFFECT; GENE MUTATION; GENE SEQUENCE; GENETIC VARIABILITY; HAPLOTYPE; HUMAN; LIPID METABOLISM; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RIEGER SYNDROME; SINGLE NUCLEOTIDE POLYMORPHISM; STEROID METABOLISM;

ANTERIOR EYE SEGMENT; ARYL HYDROCARBON HYDROXYLASES; BASE SEQUENCE; EYE ABNORMALITIES; FOUNDER EFFECT; GLAUCOMA; HAPLOTYPES; HUMANS; MICROSATELLITE REPEATS; MUTATION;

EID: 33646892373     PISSN: 10900535     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

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