Myasthenic syndrome caused by mutation of the SCN4A sodium channel

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

Volumn 100, Issue 12, 2003, Pages 7377-7382

  Tsujino, Akira ^a   Maertenst, Chantal ^b   Ohno, Kinji ^a   Shen, Xin Ming ^a   Fukuda, Taku ^a   Harper, C Michael ^a   Cannon, Stephen C ^c   Engel, Andrew G ^a  

^a MAYO CLINIC   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

^c UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; DNA; ION CHANNEL; SODIUM CHANNEL; SODIUM ION;

ADULT; ARTICLE; CASE REPORT; CONTROLLED STUDY; FEMALE; GENE; GENE MUTATION; HAPLOTYPE; HISTOLOGY; HUMAN; HUMAN TISSUE; MEMBRANE POTENTIAL; MUSCLE; MUSCLE ACTION POTENTIAL; MYASTHENIA; NERVE STIMULATION; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SCN4A GENE; SYNAPTIC POTENTIAL; SYNDROME DELINEATION;

ADULT; BASE SEQUENCE; CASE-CONTROL STUDIES; CELL LINE; DNA, COMPLEMENTARY; ELECTRIC STIMULATION; FEMALE; HUMANS; MOLECULAR SEQUENCE DATA; MOTOR ENDPLATE; MYASTHENIC SYNDROMES, CONGENITAL; PHENOTYPE; POINT MUTATION; RECOMBINANT PROTEINS; SODIUM CHANNELS;

EID: 0037794423     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.1230273100     Document Type: Article

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