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Volumn 51, Issue 1, 2002, Pages 102-112
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Novel delta subunit mutation in slow-channel syndrome causes severe weakness by novel mechanisms
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Author keywords
[No Author keywords available]
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Indexed keywords
ION CHANNEL;
ADOLESCENT;
ARTICLE;
CASE REPORT;
GENE EXPRESSION;
GENE MUTATION;
GENETIC LINKAGE;
HUMAN;
MALE;
MUSCLE WEAKNESS;
MYASTHENIA;
OOCYTE;
PATHOGENESIS;
PRIORITY JOURNAL;
SYNAPTIC TRANSMISSION;
XENOPUS;
ADOLESCENT;
AMINO ACID SEQUENCE;
ANIMALS;
CHILD;
ELECTROMYOGRAPHY;
HUMANS;
ION CHANNEL GATING;
MALE;
MOLECULAR SEQUENCE DATA;
MOTOR ENDPLATE;
MUSCLE WEAKNESS;
MUTAGENESIS, SITE-DIRECTED;
MYASTHENIC SYNDROMES, CONGENITAL;
NEUROMUSCULAR JUNCTION;
OOCYTES;
PATCH-CLAMP TECHNIQUES;
POINT MUTATION;
RECEPTORS, NICOTINIC;
XENOPUS;
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EID: 0036135172
PISSN: 03645134
EISSN: None
Source Type: Journal
DOI: 10.1002/ana.10077 Document Type: Article |
Times cited : (60)
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References (30)
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