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Genetic defects disrupting glial ion and water homeostasis in the brain

  • Published:2018-05 Issue:3 Volume:28 Page:372-387
  • ISSN:1015-6305
  • Container-title:Brain Pathology
  • language:en
  • Short-container-title:Brain Pathology

Author:

Min Rogier12ORCID,van der Knaap Marjo S.13

Affiliation:

1. Department of Child Neurology, Amsterdam Neuroscience; VU University Medical Center; Amsterdam The Netherlands

2. Department of Integrative Neurophysiology; Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University; Amsterdam The Netherlands

3. Department of Functional Genomics; Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University; Amsterdam The Netherlands

Funder

E-Rare

Hersenstichting

Publisher

Wiley

Subject

Neurology (clinical),Pathology and Forensic Medicine,General Neuroscience

Reference160 articles.

1. Diseases of connexins expressed in myelinating glia;Abrams;Neurosci Lett,2017

2. GJB1-associated X-linked Charcot-Marie-Tooth disease, a disorder affecting the central and peripheral nervous systems;Abrams;Cell Tissue Res,2015

3. A new mutation in GJC2 associated with subclinical leukodystrophy;Abrams;J Neurol,2014

4. Brain MR in Fukuyama congenital muscular dystrophy;Aida;AJNR Am J Neuroradiol,1996

5. A wide clinical phenotype spectrum in patients with ATP1A2 mutations;Al-Bulushi;J Child Neurol,2014

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