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Journal of Cell Science|September 13, 2005
Basolateral localization of native ClC-2 chloride channels in absorptive intestinal epithelial cells and basolateral sorting encoded by a CBS-2 domain di-leucine motifGaspar Peña-Münzenmayer, Marcelo Catalán, Isabel Cornejo, et al.
Human Mutation|May 25, 2013
Novel CLCNKB mutations causing Bartter syndrome affect channel surface expressionMathilde Keck, Olga Andrini, Olivier Lahuna, et al.
Nature Genetics|September 12, 2006
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPaseAlfredo Ramirez, André Heimbach, Jan Gründemann, et al.
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