Phenotypic Variability in a Mexican Mestizo Family with Retinal Vasculopathy with Cerebral Leukodystrophy and TREX1 Mutation p.V235Gfs*6-Reference-Cited by-同舟云学术

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Phenotypic Variability in a Mexican Mestizo Family with Retinal Vasculopathy with Cerebral Leukodystrophy and TREX1 Mutation p.V235Gfs*6

Published:2018-04-26 Issue:2 Volume:70 Page:
ISSN:0034-8376
Container-title:Revista de investigaci�n Cl�nica
language:en
Short-container-title:RIC

Author:

Monroy-Jaramillo Nancy,Cerón Aurelio,León Elizabeth,Rivas Verónica,Ochoa-Morales Adriana,Arteaga-Alcaraz María Georgina,Nocedal-Rustrian Fausto Carlos,Gallegos Cecilia,Alonso-Vilatela María Elisa,Corona Teresa,Flores José

Publisher

Publicidad Permanyer, SLU

Subject

General Medicine

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. TREX1 p.A129fs and p.Y305C variants in a large multi-ethnic cohort of CADASIL-like unrelated patients;Neurobiology of Aging;2023-03

2. A case of retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations: Long‐term treatment with repeated courses of immunotherapy;Neurology and Clinical Neuroscience;2022-09-07

3. Tumor-Like Brain Lesions Associated With Variants of Uncertain Significance Compared to Previous Studies: A Case Report;Cureus;2022-07-14

4. Retinal Vasculopathy with Cerebral Leukoencephalopathy and Systemic manifestations (RVCL-S): An update on basic science and clinical perspectives;Cerebral Circulation - Cognition and Behavior;2022

5. Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis;PLOS Genetics;2021-10-18

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