A mutation in autosomal dominant myotonia congenita affects pore properties of the muscle chloride channel

Proceedings of the National Academy of Sciences of the United States of America

Volumn 94, Issue 6, 1997, Pages 2729-2734

  Fahlke, Christoph ^a   Beck, Carol L ^a   George Jr , Alfred L ^a  

^a VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

CLCN1; electrophysiology; permeation; skeletal muscle

Indexed keywords

CHLORIDE CHANNEL; CHLORIDE ION;

ANIMAL CELL; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CELL MEMBRANE PERMEABILITY; GENE MUTATION; ION CONDUCTANCE; NONHUMAN; PRIORITY JOURNAL; SKELETAL MUSCLE; THOMSEN DISEASE;

ANIONS; CELL LINE; CHLORIDE CHANNELS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 7; GENES, DOMINANT; HUMANS; IODIDES; MEMBRANE POTENTIALS; MUSCLE, SKELETAL; MYOTONIA CONGENITA; PATCH-CLAMP TECHNIQUES; POINT MUTATION; RECOMBINANT PROTEINS; TIME FACTORS; TRANSFECTION;

ANIMALIA; MAMMALIA;

EID: 0030975478     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.94.6.2729     Document Type: Article

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