Molecular screening for CYP1B1 gene mutations and phenotypic variability in Mexican primary congenital glaucoma patients

被引：0
|
作者：
de Rivera, ON
Rodríguez, S
Vázquez, O
Morán, V
Korder, V
Hartlebem, K
机构：
[1] IPN, Ctr Invest Cienica & Aplicada & Tecnol Avanzada, Mexico City 07738, DF, Mexico
[2] Inst Oftalmol Conde Valenciana, Unidad Invest Genet & Biol Mol, Mexico City, DF, Mexico
[3] Inst Oftalmol Conde Valenciana, Dept Glaucoma, Mexico City, DF, Mexico
来源：
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 2004年 / 45卷
关键词：
D O I：
暂无
中图分类号：
R77 [眼科学];
学科分类号：
100212 ;
摘要：
4407
引用
收藏
页码：U438 / U438
页数：1
相关论文
共 50 条
  • [1] CYP1B1 mutations in Spanish patients with primary congenital glaucoma: phenotypic and functional variability
    Campos-Mollo, Ezequiel
    Lopez-Garrido, Maria-Pilar
    Blanco-Marchite, Cristina
    Garcia-Feijoo, Julian
    Peralta, Jesus
    Belmonte-Martinez, Jose
    Ayuso, Carmen
    Escribano, Julio
    MOLECULAR VISION, 2009, 15 (42): : 417 - 431
  • [2] Screening of West Siberian patients with primary congenital glaucoma for CYP1B1 gene mutations
    Ivanoshchuk, D. E.
    Mikhailova, S., V
    Fenkova, O. G.
    Shakhtshneider, E., V
    Fursova, A. Z.
    Bychkov, I. Y.
    Voevoda, M., I
    VAVILOVSKII ZHURNAL GENETIKI I SELEKTSII, 2020, 24 (08): : 861 - 867
  • [3] Geographical Variability in CYP1B1 Mutations in Primary Congenital Glaucoma
    Shah, Manali
    Bouhenni, Rachida
    Benmerzouga, Imaan
    JOURNAL OF CLINICAL MEDICINE, 2022, 11 (07)
  • [4] CYP1B1 mutations in patients with primary congenital glaucoma
    Sitorus, RS
    Preising, MN
    Ardjo, SM
    Lorenz, B
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2002, 43 : U961 - U961
  • [5] Clinical Variability of Primary Congenital Glaucoma in a Spanish Family With Cyp1b1 Gene Mutations
    Morales-Fernandez, Laura
    Martinez-de-la-Casa, Jose M.
    Garcia-Bella, Javier
    Mendez, Carmen
    Saenz-Frances, Federico
    Garcia, Maite
    Escribano, Julio
    Garcia-Feijoo, Julian
    JOURNAL OF GLAUCOMA, 2015, 24 (08) : 630 - 634
  • [6] Targeted Screening for Predominant CYP1B1 Mutations in Primary Congenital Glaucoma
    Sarfarazi, Mansoor
    JOURNAL OF OPHTHALMIC & VISION RESEARCH, 2018, 13 (04) : 373 - 375
  • [7] CYP1B1 Gene Mutations Causing Primary Congenital Glaucoma in Tunisia
    Bouyacoub, Yosra
    Ben Yahia, Salim
    Abroug, Nesrine
    Kahloun, Rim
    Kefi, Rym
    Khairallah, Moncef
    Abdelhak, Sonia
    ANNALS OF HUMAN GENETICS, 2014, 78 (04) : 255 - 263
  • [8] Molecular analysis of CYP1B1 gene in patients affected by primary congenital glaucoma
    Giuffre, I
    Lando, G
    Penco, S
    Manfredini, E
    Piozzi, E
    Marocchi, A
    Patrosso, MC
    Maselli, E
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2004, 45 : U437 - U437
  • [9] Molecular analysis of the CYP1B1 gene:: Identification of novel truncating mutations in patients with primary congenital glaucoma
    Messina-Baas, O. M.
    Gonzalez-Huerta, L. M.
    Chima-Galan, C.
    Kofman-Alfaro, S. H.
    Rivera-Vega, M. R.
    Babayan-Mena, I.
    Cuevas-Covarrubias, S. A.
    OPHTHALMIC RESEARCH, 2007, 39 (01) : 17 - 23
  • [10] Meta-analysis of CYP1B1 gene mutations in primary congenital glaucoma patients
    Haddad, Amine
    Ait Boujmia, Oum Kaltoum
    El Maaloum, Loubna
    Dehbi, Hind
    EUROPEAN JOURNAL OF OPHTHALMOLOGY, 2021, 31 (06) : 2796 - 2807
12345