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Summary Anatomy Item Literature (521) Expression Attributions Wiki
XB-ANAT-3595

Papers associated with basal ganglion (and slc12a6)

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SLC12A ion transporter mutations in sporadic and familial human congenital hydrocephalus., Jin SC., Mol Genet Genomic Med. September 1, 2019; 7 (9): e892.    

Potassium-chloride cotransporter 3 interacts with Vav2 to synchronize the cell volume decrease response with cell protrusion dynamics., Salin-Cantegrel A., PLoS One. May 15, 2013; 8 (5): e65294.            

Transit defect of potassium-chloride Co-transporter 3 is a major pathogenic mechanism in hereditary motor and sensory neuropathy with agenesis of the corpus callosum., Salin-Cantegrel A., J Biol Chem. August 12, 2011; 286 (32): 28456-65.

HMSN/ACC truncation mutations disrupt brain-type creatine kinase-dependant activation of K+/Cl- co-transporter 3., Salin-Cantegrel A., Hum Mol Genet. September 1, 2008; 17 (17): 2703-11.

Distal truncation of KCC3 in non-French Canadian HMSN/ACC families., Salin-Cantegrel A., Neurology. September 25, 2007; 69 (13): 1350-5.

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