Physiology and pathophysiology of CLC-1: Mechanisms of a chloride channel disease, myotonia

Journal of Biomedicine and Biotechnology

Volumn 2011, Issue , 2011, Pages

  Tang, Chih Yung ^a   Chen, Tsung Yu ^b  

^a NATIONAL TAIWAN UNIVERSITY   (Taiwan)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE; CHLORIDE; CHLORIDE CHANNEL; CHLORIDE CHANNEL 1; GLUTAMIC ACID; POTASSIUM ION; UNCLASSIFIED DRUG; VOLTAGE GATED SODIUM CHANNEL; CLC 1 CHANNEL; CLC-1 CHANNEL;

BECKER MUSCULAR DYSTROPHY; BIOPHYSICS; CELL MEMBRANE; CHANNEL GATING; CHLORIDE CHANNELOPATHY; CHROMOSOME 7; GENE MUTATION; HUMAN; MEMBRANE TRANSPORT; MOLECULAR BIOLOGY; MOLECULAR PATHOLOGY; MUSCLE FUNCTION; MUTAGENESIS; MYOTONIA; NONHUMAN; PROTEIN EXPRESSION; PROTEIN STRUCTURE; PROTEIN SYNTHESIS; PROTEIN TRANSPORT; REVIEW; SKELETAL MUSCLE; THOMSEN DISEASE; ANIMAL; CHEMICAL STRUCTURE; FEMALE; GENETICS; MALE; MUTATION; PATHOPHYSIOLOGY; PHYSIOLOGY;

ANIMALS; CHLORIDE CHANNELS; FEMALE; HUMANS; MALE; MODELS, MOLECULAR; MUTATION; MYOTONIA CONGENITA;

EID: 84862954608     PISSN: 11107243     EISSN: 11107251     Source Type: Journal    
DOI: 10.1155/2011/685328     Document Type: Review

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