CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes.
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Genetic, Biochemical and Clinical Insights into Primary Congenital GlaucomaGenotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and BrazilMutational spectrum of the CYP1B1 gene in Pakistani patients with primary congenital glaucoma: novel variants and genotype-phenotype correlations.Screening of CYP1B1 and MYOC in Moroccan families with primary congenital glaucoma: three novel mutations in CYP1B1.CYP1B1 mutations in patients with primary congenital glaucoma from Saudi Arabia.Carrier frequency of CYP1B1 mutations in the United States (an American Ophthalmological Society thesis).Screening of CYP1B1 and LTBP2 genes in Saudi families with primary congenital glaucoma: genotype-phenotype correlation.Glaucoma in iran and contributions of studies in iran to the understanding of the etiology of glaucoma.Functional and Structural Analyses of CYP1B1 Variants Linked to Congenital and Adult-Onset Glaucoma to Investigate the Molecular Basis of These Diseases.Myocilin mutations are not a major cause of primary congenital glaucoma in Iranian patients.Sex Bias in Primary Congenital Glaucoma Patients with and without CYP1B1 Mutations.Contributions of MYOC and CYP1B1 mutations to JOAGNovel CYP1B1 mutations in consanguineous Pakistani families with primary congenital glaucoma.Screening of common CYP1B1 mutations in Iranian POAG patients using a microarray-based PrASE protocolA spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent.Genotyping results of Iranian PCG families suggests one or more PCG locus other than GCL3A, GCL3B, and GCL3C existPrimary Congenital Glaucoma and the Involvement of CYP1B1.CYP1B1 gene mutations with incomplete penetrance in a Chinese pedigree with primary congenital glaucoma: a case report and review of literatures.CYP1B1 gene mutations causing primary congenital glaucoma in Tunisia.Primary congenital and developmental glaucomas.Novel gene mutations causing primary congenital glaucoma.Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma.Analysis of CYP1B1 Gene Mutations in Patients with Primary Congenital Glaucoma.Genotype/Phenotype Correlation in Primary Congenital Glaucoma Patients in the Lebanese Population: A Pilot Study.
P2860
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P2860
CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
CYP1B1 mutation profile of Ira ...... nts and associated haplotypes.
@ast
CYP1B1 mutation profile of Ira ...... nts and associated haplotypes.
@en
type
label
CYP1B1 mutation profile of Ira ...... nts and associated haplotypes.
@ast
CYP1B1 mutation profile of Ira ...... nts and associated haplotypes.
@en
prefLabel
CYP1B1 mutation profile of Ira ...... nts and associated haplotypes.
@ast
CYP1B1 mutation profile of Ira ...... nts and associated haplotypes.
@en
P2093
P2860
P1476
CYP1B1 mutation profile of Ira ...... ents and associated haplotypes
@en
P2093
Akram Rismanchian
Ali Abdolahi
Ali R Lasheyee
Behnam Ghafarzadeh
Behnaz Bayat
Betsabeh Khoramian Tusi
Elahe Elahi
Fereshteh Chitsazian
Heidar Amini Saroei
Mahmood Jabbarvand
P2860
P304
P356
10.2353/JMOLDX.2007.060157
P577
2007-07-01T00:00:00Z