Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families
SourceAmerican Journal of Human Genetics, 56, 2, (1995), pp. 374-380
Article / Letter to editor
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American Journal of Human Genetics
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