A novel homozygous mutation of CLCN2 in a patient with characteristic brain MRI images – A first case of CLCN2-related leukoencephalopathy in Japan - ScienceDirect
Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies | Nature Genetics
CLCN2 - Wikipedia
CLCN2 chloride channel mutations in familial hyperaldosteronism type II | Nature Genetics
Biallelic CLCN2 mutations cause retinal degeneration by impairing retinal pigment epithelium phagocytosis and chloride channel function | SpringerLink
A CLCN2 variant identified in a patient with early-onset primary... | Download Scientific Diagram
Animals | Free Full-Text | Two Different Copy Number Variations of the CLCN2 Gene in Chinese Cattle and Their Association with Growth Traits
A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism | Nature Genetics
CLCN2-related leukoencephalopathy: a case report and review of the literature | BMC Neurology | Full Text
Figure 1. [MRI of an individual age...]. - GeneReviews® - NCBI Bookshelf
ClC-2 increases aldosterone synthase expression in H295R cells a, RNA... | Download Scientific Diagram
A case of CLCN2-related leukoencephalopathy with bright tree appearance during aseptic meningitis - ScienceDirect
CLCN2 Antibody (ABIN951555)
Brain white matter oedema due to ClC-2 chloride channel deficiency: an observational analytical study - The Lancet Neurology