Asociación entre la mutación homocigota c.318A>T en el exón 2 del gen EIF2B5 y la forma infantil de la leucoencefalopatía con sustancia blanca evanescente-Reference-Cited by-同舟云学术

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Asociación entre la mutación homocigota c.318A>T en el exón 2 del gen EIF2B5 y la forma infantil de la leucoencefalopatía con sustancia blanca evanescente

Published:2017-09 Issue:5 Volume:74 Page:364-369
ISSN:1665-1146
Container-title:Boletín Médico del Hospital Infantil de México
language:es
Short-container-title:Boletín Médico del Hospital Infantil de México

Author:

Esmer Carmen,Blanco Hernández Gabriela,Saavedra Alanís Víctor,Reyes Vaca Jorge Guillermo,Bravo Oro Antonio

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference30 articles.

1. Defining and categorizing leukoencephalopathies of unknown origin: MR imaging approach;van der Knaap;Radiology.,1999

2. Vanishing white matter disease;van der Knaap;Lancet Neurol.,2006

3. Polycystische umwandlung des marklagers mit progredientem verlauf. Atypische diffuse sklerose?;Eicke;Arch Psychiat Nervenkr.,1962

4. The spectrum of mutations for the diagnosis of vanishing white matter disease;Scali;Neurol Sci.,2006

5. Vanishing white matter disease: a review with focus on its genetics;Pronk;Ment Retard Dev Disabil Res Rev.,2006

Cited by 3 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. Adult-Onset White Matter Vanishing Disease With Ovarian Failure in a Salvadoran Patient;Cureus;2023-06-03

2. EIF2B2 gene mutation causing early onset vanishing white matter disease: a case report;Italian Journal of Pediatrics;2022-07-27

3. Low EIF2B5 expression predicts poor prognosis in ovarian cancer;Medicine;2020-01

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