A Tunisian patient with CLCN2 ‐related leukoencephalopathy
Author:
Affiliation:
1. Molecular Neurobiology and Neuropathology Department National Institute Mongi Ben Hamida of Neurology La Rabta Tunisia
2. Laboratoire Procédés de Criblage Moléculaire et Cellulaire Centre de Biotechnologie de Sfax Sfax Tunisia
Publisher
Wiley
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.6737
Reference9 articles.
1. A novel homozygous change ofCLCN2(p.His590Pro) is associated with a subclinical form of leukoencephalopathy with ataxia (LKPAT)
2. CLCN2-related leukoencephalopathy: a case report and review of the literature
3. A novel homozygous mutation of CLCN2 in a patient with characteristic brain MRI images – A first case of CLCN2-related leukoencephalopathy in Japan
4. Male germ cells and photoreceptors, both dependent on close cell–cell interactions, degenerate upon ClC-2 Cl− channel disruption
5. Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation
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