A Novel Frameshift Mutation in SLC2A1 Associated with a Mild form of Glucose Transporter Type 1-Related Movement Disorder-Reference-Cited by-同舟云学术

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A Novel Frameshift Mutation in SLC2A1 Associated with a Mild form of Glucose Transporter Type 1-Related Movement Disorder

Published:2015-08-07 Issue:02 Volume:13 Page:088-091
ISSN:1304-2580
Container-title:Journal of Pediatric Neurology
language:en
Short-container-title:J Pediatr Neurol

Author:

Awaad Yasser¹,Berry Ian²,Elsayed Solaf³,Tomoum Hoda⁴

Affiliation:

1. Department of Pediatric Neurology, National Neurosciences Institute, King Fahad Medical City, King Abdulaziz Bin Saud University, Riyadh, Saudi Arabia

2. Yorkshire Regional Genetics Service, DNA Laboratory, Ashley Wing, St James's University Hospital, United Kingdom

3. Medical Genetics Center and Genetics Unit, Department of Pediatrics, Ain Shams University, Cairo, Egypt

4. Department of Pediatrics, Ain Shams University, Cairo, Egypt

Publisher

Georg Thieme Verlag KG

Subject

Clinical Neurology,Pediatrics, Perinatology, and Child Health

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0035-1556765.pdf

Cited by 1 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. The diagnostic and prognostic role of cerebrospinal fluid biomarkers in glucose transporter 1 deficiency: a systematic review;European Journal of Pediatrics;2024-07-02

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