Sporadic Cases with Novel Mutations and Pedigree in Hereditary Leukoencephalopathy with Axonal Spheroids-Reference-Cited by-同舟云学术

Sporadic Cases with Novel Mutations and Pedigree in Hereditary Leukoencephalopathy with Axonal Spheroids

Published:2017-02-03 Issue:3 Volume:56 Page:893-898
ISSN:1387-2877
Container-title:Journal of Alzheimer's Disease
language:
Short-container-title:JAD

Author:

Wu Liyong¹,Liu Jia¹,Sha Longze²,Wang Xianling¹,Li Jieying¹,Dong Jing¹,Jia Jianping¹

Affiliation:

1. Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China

2. National Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences & Neuroscience Center, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China

Publisher

IOS Press

Subject

Psychiatry and Mental health,Geriatrics and Gerontology,Clinical Psychology,General Medicine,General Neuroscience

Reference18 articles.

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2. De novo mutations in hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS);Karle;Neurology,2013

3. Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids;Rademakers;Nat Genet,2011

4. Hereditary diffuse leukoencephalopathy with axonal spheroids: Three patients with stroke-like presentation carrying new mutations in the CSF1R gene;Battisti;J Neurol,2014

5. Early pathologic changes in hereditary diffuse leukoencephalopathy with spheroids;Riku;J Neuropathol Exp Neurol,2014

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