Associated Papers
Dent's disease: An unusual cause of kidney failure.
Leite de Sousa L et al.
Clinical Nephrology. Case Studies, 2023
ClC-5 mutations associated with Dent's disease: a major role of the dimer interface.
Lourdel S et al.
Pflugers Archiv : European Journal of Physiology, 2012
Heterogeneity in the processing of CLCN5 mutants related to Dent disease.
Grand T et al.
Human Mutation, 2011
Characterization of Dent's disease mutations of CLC-5 reveals a correlation between functional and cell biological consequences and protein structure.
Smith AJ et al.
American Journal of Physiology. Renal Physiology, 2009
Functional evaluation of Dent's disease-causing mutations: implications for ClC-5 channel trafficking and internalization.
Ludwig M et al.
Human Genetics, 2005
Modeling study of human renal chloride channel (hCLC-5) mutations suggests a structural-functional relationship.
Wu F et al.
Kidney International, 2003
Select a paper to view details