Multimeric structure of CIC-1 chloride channel revealed by mutations in dominant myotonia congenita (Thomsen)

EMBO Journal

Volumn 13, Issue 4, 1994, Pages 737-743

  Steinmeyer, Klaus ^a   Lorenz, Claudius ^a   Pusch, Michael ^a   Koch, Manuela C ^b   Jentsch, Thomas J ^a  

^a UNIVERSITY OF HAMBURG   (Germany)

^b PHILIPPS UNIVERSITY MARBURG   (Germany)

Author keywords

Anion channel; Human genetics; Muscle; Myotonia; Voltage gated

Indexed keywords

CHLORIDE CHANNEL; MONOMER; OLIGOMER; PROTEIN SUBUNIT; COMPLEMENTARY DNA;

ARTICLE; BIOASSAY; CELL KINETICS; CELL VOLUME; EPITHELIUM; GENE EXPRESSION REGULATION; GENE MUTATION; HUMAN; HUMAN CELL; MEMBRANE TRANSPORT; MUSCLE EXCITATION; POLYMERIZATION; PRIORITY JOURNAL; THOMSEN DISEASE; AMINO ACID SEQUENCE; ANIMAL; CELL LINE; CHEMISTRY; CHLORIDE CHANNEL; DOMINANT GENE; FEMALE; GENETICS; MALE; MOLECULAR CLONING; MOLECULAR GENETICS; MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; PROTEIN CONFORMATION; SEQUENCE HOMOLOGY;

AMINO ACID SEQUENCE; ANIMAL; BASE SEQUENCE; CELL LINE; CHLORIDE CHANNELS; CLONING, MOLECULAR; DNA, COMPLEMENTARY; FEMALE; GENES, DOMINANT; HUMAN; MALE; MOLECULAR SEQUENCE DATA; MUTATION; MYOTONIA CONGENITA; PEDIGREE; PROTEIN CONFORMATION; SEQUENCE HOMOLOGY, AMINO ACID; SUPPORT, NON-U.S. GOV'T;

EID: 0028032140     PISSN: 02614189     EISSN: None     Source Type: Journal    
DOI: 10.1002/j.1460-2075.1994.tb06315.x     Document Type: Article

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