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The Journal of Clinical Investigation|March 1, 1997
Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5)S E Lloyd, S H Pearce, W Günther, et al.The Journal of Physiology|March 14, 2000
Inhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M1 muscarinic acetylcholine receptorsA A Selyanko, J K Hadley, I C Wood, et al.Science (New York, N.Y.)|February 7, 1998
A potassium channel mutation in neonatal human epilepsyC Biervert, B C Schroeder, C Kubisch, et al.Journal of Medical Genetics|November 1, 1993
Evidence for genetic homogeneity in autosomal recessive generalised myotonia (Becker)M C Koch, K Ricker, M Otto, et al.Cell|February 20, 1999
KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafnessC Kubisch, B C Schroeder, T Friedrich, et al.Cell|February 24, 2001
Loss of the ClC-7 chloride channel leads to osteopetrosis in mice and manU Kornak, D Kasper, M R Bösl, et al.Human Molecular Genetics|August 15, 2000
Mutations in the a3 subunit of the vacuolar H(+)-ATPase cause infantile malignant osteopetrosisU Kornak, A Schulz, W Friedrich, et al.Neurology|May 5, 1998
Novel muscle chloride channel (CLCN1) mutations in myotonia congenita with various modes of inheritance including incomplete dominance and penetranceE Plassart-Schiess, A Gervais, B Eymard, et al.Bone|October 10, 2013
ClC-7 expression levels critically regulate bone turnover, but not gastric acid secretionC Supanchart, L Wartosch, C Schlack, et al.Science (New York, N.Y.)|August 7, 1992
The skeletal muscle chloride channel in dominant and recessive human myotoniaM C Koch, K Steinmeyer, C Lorenz, et al.Pageof 10