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.
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R. Ophoff | B. Echenne | A. Elbaz | K. Jurkat-Rott | R. Ophoff | T. Links | B. Fontaine | J. Guimarães | J. Saudubray | N. Monnier | M. Fardeau | H. Nivet | J. Vale-Santos | R. Frants | N. Feingold | P. Lapie | C. Piussan | G. Padberg | G. Lenoir | B. Bady | A. Vila | Frank Lehmann‐Horn | F. Lehmann‐Horn | K. Abe | van der Johannes Hoeven | Ar Wintzen | Jp Grunfeld | Jp. Grunfeld