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Human Molecular Genetics|September 16, 1998
ClC-1 chloride channel mutations in myotonia congenita: variable penetrance of mutations shifting the voltage dependenceC Kubisch, T Schmidt-Rose, B Fontaine, et al.
Genetical Research|October 1, 1995
Chloride channel 2 gene (Clc2) maps to chromosome 16 of the mouse, extending a region of conserved synteny with human chromosome 3qA Lengeling, M Gronemeier, M Ronsiek, et al.
The Journal of Biological Chemistry|February 25, 1994
Nonsense and missense mutations in the muscular chloride channel gene Clc-1 of myotonic miceM Gronemeier, A Condie, J Prosser, et al.
The American Journal of Physiology|May 1, 1997
Localization and induction by dehydration of ClC-K chloride channels in the rat kidneyA Vandewalle, F Cluzeaud, M Bens, et al.
American Journal of Human Genetics|December 1, 1995
Spectrum of mutations in the major human skeletal muscle chloride channel gene (CLCN1) leading to myotoniaC Meyer-Kleine, K Steinmeyer, K Ricker, et al.
Neuroscience|September 18, 2007
Detection and differentiation of sensorineural hearing loss in mice using auditory steady-state responses and transient auditory brainstem responsesD Pauli-Magnus, G Hoch, N Strenzke, et al.
The Journal of General Physiology|June 20, 1998
Permeation and block of the skeletal muscle chloride channel, ClC-1, by foreign anionsG Y Rychkov, M Pusch, M L Roberts, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 27, 2001
Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channelK Dedek, B Kunath, C Kananura, et al.
Neuron|June 8, 2001
Disruption of KCC2 reveals an essential role of K-Cl cotransport already in early synaptic inhibitionC A Hübner, V Stein, I Hermans-Borgmeyer, et al.
Human Molecular Genetics|September 25, 1997
Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmiasB Wollnik, B C Schroeder, C Kubisch, et al.
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