Clinical and genetic characterization of adult‐onset leukoencephalopathy caused by CSF1R mutations-Reference-Cited by-同舟云学术

Clinical and genetic characterization of adult‐onset leukoencephalopathy caused by CSF1R mutations

Published:2021-10-15 Issue:11 Volume:8 Page:2121-2131
ISSN:2328-9503
Container-title:Annals of Clinical and Translational Neurology
language:en
Short-container-title:Ann. Clin. Transl. Neurol.

Author:

Tsai Pei‐Chien¹,Fuh Jong‐Ling²³⁴,Yang Chih‐Chao⁵,Chang Anna⁶,Lien Li‐Ming⁶,Wang Pei‐Ning²³⁴,Lai Kuan‐Lin²³⁴,Tsai Yu‐Shuen⁷,Lee Yi‐Chung²³⁴,Liao Yi‐Chu²³⁴^ORCID

Affiliation:

1. Department of Life Sciences National Chung Hsing University Taichung Taiwan

2. Department of Neurology Taipei Veterans General Hospital Taipei Taiwan

3. Faculty of Medicine School of Medicine National Yang Ming Chiao Tung University Taipei Taiwan

4. Brain Research Center National Yang Ming Chiao Tung University Taipei Taiwan

5. Department of Neurology National Taiwan University Hospital Taipei Taiwan

6. Department of Neurology Shin Kong Wu Ho‐Su Memorial Hospital Taipei Taiwan

7. Center for Systems and Synthetic Biology National Yang Ming Chiao Tung University Taipei Taiwan

Funder

Ministry of Science and Technology, Taiwan

Ministry of Education

Publisher

Wiley

Subject

Clinical Neurology,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/acn3.51467

Reference49 articles.

1. Adult onset leukodystrophy with neuroaxonal spheroids and pigmented glia: report of a family, historical perspective, and review of the literature

2. CSF1R mutations link POLD and HDLS as a single disease entity

3. CSF1R-related leukoencephalopathy

4. Clinical and genetic characterization of adult-onset leukoencephalopathy with axonal spheroids and pigmented glia associated withCSF1Rmutation

5. Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids

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