CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes

Journal of Molecular Diagnostics

Volumn 9, Issue 3, 2007, Pages 382-393

  Chitsazian, Fereshteh ^a,b   Tusi, Betsabeh Khoramian ^a,b   Elahi, Elahe ^a,b   Saroei, Heidar Amini ^c   Sanati, Mohammad H ^a   Yazdani, Shahin ^d   Pakravan, Mohammad ^d   Nilforooshan, Navid ^e   Eslami, Yadollah ^c   Zare Mehrjerdi, Mohammad Ali ^c   Zareei, Reza ^c   Jabbarvand, Mahmood ^c   Abdolahi, Ali ^c   Lasheyee, Ali R ^c   Etemadi, Arash ^c   Bayat, Behnaz ^a   Sadeghi, Mehdi ^a,b   Banoei, Mohammad M ^a   Ghafarzadeh, Behnam ^f   Rohani, Mohammad R ^f   Rismanchian, Akram ^g   Thorstenson, Yvonne ^h   Sarfarazi, Mansoor ⁱ   more..

^a NATIONAL INSTITUTE OF GENETIC ENGINEERING AND BIOTECHNOLOGY   (Iran)

^b UNIVERSITY OF TEHRAN   (Iran)

^c TEHRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^d SHAHID BEHESHTI UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^e IRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^f ZAHEDAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^g ISFAHAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^h STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

ⁱ UNIVERSITY OF CONNECTICUT HEALTH CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME P450 1B1;

3' UNTRANSLATED REGION; 5' UNTRANSLATED REGION; ALLELE; ARTICLE; COMPUTER PROGRAM; CONGENITAL GLAUCOMA; CONTROLLED STUDY; FRAMESHIFT MUTATION; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC HETEROGENEITY; GENETIC VARIABILITY; GENOTYPE PHENOTYPE CORRELATION; HAPLOTYPE MAP; HUMAN; IRAN; MAJOR CLINICAL STUDY; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SEQUENCE ALIGNMENT; SEQUENCE ANALYSIS; SEQUENCE HOMOLOGY; SINGLE NUCLEOTIDE POLYMORPHISM; STOP CODON;

EID: 34548189984     PISSN: 15251578     EISSN: None     Source Type: Journal    
DOI: 10.2353/jmoldx.2007.060157     Document Type: Article

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