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FOXC2, PITX2 and CYP1B1 variants identified in congenital glaucoma patients.

Name: FOXC2, PITX2 and CYP1B1 variants identified in congenital glaucoma patients.
Published: 2019-01-18T18:26:25+00:00
License: https://creativecommons.org/licenses/by/4.0/
Keywords: subcellular localization analyses, modifier factors, PITX 2, 133 CG families, PCG, PITX 2 variants increase, glaucoma Congenital glaucoma, FOXC 2, .1183C, CYP 1B glaucoma-associated genotypes, FOXC 2 variants, PITX 2 variants, .535C, transactivation luciferase reporter assays, 25 CG cases, Transactivation reporter analyses

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posted on 2019-01-18, 18:26 authored by Cristina Medina-Trillo, José-Daniel Aroca-Aguilar, Jesús-José Ferre-Fernández, Susana Alexandre-Moreno, Laura Morales, Carmen-Dora Méndez-Hernández, Julián García-Feijoo, Julio Escribano

FOXC2, PITX2 and CYP1B1 variants identified in congenital glaucoma patients.

FOXC2, PITX2 and CYP1B1 variants identified in congenital glaucoma patients.

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