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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Publication year
1995
Author(s)
Elbaz, A.
Vale-Santos, J.
Jurkat-Rott, K.
Lapie, P.
Ophoff, R.A.
Bady, B.
Links, T.P.
Piussan, C.
Vila, A.
Monnier, N.
Padberg, G.W.A.M.
Feingold, N.
Guimaraes, J.
Wintzen, A.R.
Hoeven, J.H. van
Saudubray, J.M.
Grunfeld, J.P.
Lenoir, G.
Nivet, H.
Echenne, B.
Frants, R.R.
Fardeau, M.
Lehmann-Horn, F.
Fontaine, B.
Source
American Journal of Human Genetics, 56, 2, (1995), pp. 374-380
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Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/22241   https://hdl.handle.net/2066/22241
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