What is CLCN2 Gene Epilepsy, idiopathic generalized type 11 NGS Genetic DNA Test ?
CLCN2 Antibody (NBP2-97349): Novus Biologicals
CLCN2 Antibody (ABIN560397)
A case of CLCN2-related leukoencephalopathy with bright tree appearance during aseptic meningitis - ScienceDirect
Leukoencephalopathy‐causing CLCN2 mutations are associated with impaired Cl− channel function and trafficking - Gaitán‐Peñas - 2017 - The Journal of Physiology - Wiley Online Library
CLCN2 chloride channel mutations in familial hyperaldosteronism type II | Nature Genetics
CLCN2-related leukoencephalopathy: a case report and review of the literature | BMC Neurology | Full Text
Intrinsic membrane properties of Clcn2 / pyramidal neurons are altered.... | Download Scientific Diagram
CLCN2 Antibody (ABIN560397)
CLCN2 Polyclonal Antibody (PA5-96510)
ClC-2 increases aldosterone synthase expression in H295R cells a, RNA... | Download Scientific Diagram
Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies | Nature Genetics
A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism | Nature Genetics
How a Mutated Gene Triggers Hypertension | Max Delbrück Center
Chloride Channel Protein 2 (CLCN2) Antibody | Abbexa Ltd
Gene: Clcn2 (ENSMUSG00000022843) - Summary - Mus_musculus - Ensembl genome browser 110
Cellular basis of ClC-2 Cl− channel–related brain and testis pathologies - ScienceDirect
Cellular basis of ClC-2 Cl− channel–related brain and testis pathologies - ScienceDirect
Brain white matter oedema due to ClC-2 chloride channel deficiency: an observational analytical study - The Lancet Neurology
Structure of ClC-2 and residues affected by mutations in FH-II. a... | Download Scientific Diagram
Chloride Channel Protein 2 (CLCN2) Antibody | Abbexa Ltd
Chloride Channel-2 (CLC-2, Clcn2) antibody Western C9477
CLCN2 Polyclonal Antibody, Invitrogen 100 μL; Unconjugated:Antibodies, | Fisher Scientific
CLCN2 Membrane Protein Introduction - Creative Biolabs
CLCN2 chloride channel mutations in familial hyperaldosteronism type II | Nature Genetics
