Polimorfismos del TLR4 en pacientes con enfermedad de Stargardt: un estudio familiar | Zendy

Ramses Rosales-Díaz | Zendy; Alejandro GonzálezDe la Rosa | Zendy; Nicole Macriz-Romero | Zendy; Juan Carlos Altamirano-Vallejo | Zendy; Abril Bernardette Martínez-Rizo | Zendy; Arturo Santos | Zendy; Adolfo Daniel Rodríguez-Carrizález | Zendy; José NavarroPartida | Zendy

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Polimorfismos del TLR4 en pacientes con enfermedad de Stargardt: un estudio familiar

Author(s) -

Ramses Rosales-Díaz,

Alejandro GonzálezDe la Rosa,

Nicole Macriz-Romero,

Juan Carlos Altamirano-Vallejo,

Abril Bernardette Martínez-Rizo,

Arturo Santos,

Adolfo Daniel Rodríguez-Carrizález,

José NavarroPartida

Publication year - 2019

Publication title -

revista mexicana de oftalmología

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.129

H-Index - 6

eISSN - 2604-1227

pISSN - 0187-4519

DOI - 10.24875/rmo.m20000102

Subject(s) - medicine

Purpose: Retinal pigment epithelial cells exhibit a propensity for apoptosis in Stargardt macular dystrophy (STGD). Previously, single-nucleotide polymorphisms (SNPs) in the toll-like receptor 4 (TLR4) gene have been related to apoptosis and inflammatory response. Therefore, this study was undertaken to investigate whether TLR4 SNPs are associated with STGD in a family-based

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