Molecular characterization of Axenfeld-Rieger spectrum and other anterior segment dysgeneses in a sample of Mexican patients-Reference-Cited by-同舟云学术

Molecular characterization of Axenfeld-Rieger spectrum and other anterior segment dysgeneses in a sample of Mexican patients

Published:2018-11-02 Issue:6 Volume:39 Page:728-734
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Hernández-Martínez Nancy¹,González-del Angel Ariadna¹,Alcántara-Ortigoza Miguel Angel¹,González-Huerta Luz M.²,Cuevas-Covarrubias Sergio A.²,Villanueva-Mendoza Cristina³

Affiliation:

1. Laboratorio de Biología Molecular, Instituto Nacional de Pediatría, México, México

2. Hospital General de México Dr. Eduardo Liceaga, Laboratorio de Investigación y Genética, México, México

3. Departamento de Génetica, Asociación para Evitar la Ceguera en México, México, México

Funder

Hospital Dr. Luis Sánchez Bulnes, Asociación Para Evitar la Ceguera en México, APEC and the National Institute of Pediatrics (Recursos Fiscales del Programa E022, Ciudad de México, México

Instituto Nacional de Pediatrìa

Publisher

Informa UK Limited

Subject

Genetics(clinical),Ophthalmology,Pediatrics, Perinatology, and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2018.1547911

Reference49 articles.

1. Molecular and developmental mechanisms of anterior segment dysgenesis

2. Axenfeld-Rieger syndrome

3. Duplication of MAOA, MAOB, and NDP in a patient with mental retardation and epilepsy

4. A Review of Anterior Segment Dysgeneses

5. Axenfeld–Rieger syndrome and spectrum of PITX2 and FOXC1 mutations

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