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P Lapie

Showing results (11-20 of 14) with videos related to

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Kidney International|January 1, 1996
Periodic paralysis and voltage-gated ion channelsB Fontaine, P Lapie, E Plassart, et al.
Human Genetics|November 1, 1994
Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP)E Plassart, A Elbaz, J V Santos, et al.
American Journal of Human Genetics|February 1, 1995
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 familiesA Elbaz, J Vale-Santos, K Jurkat-Rott, et al.
Human Molecular Genetics|August 1, 1994
A calcium channel mutation causing hypokalemic periodic paralysisK Jurkat-Rott, F Lehmann-Horn, A Elbaz, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Kidney International|January 1, 1996
Periodic paralysis and voltage-gated ion channelsB Fontaine, P Lapie, E Plassart, et al.
Human Genetics|November 1, 1994
Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP)E Plassart, A Elbaz, J V Santos, et al.
American Journal of Human Genetics|February 1, 1995
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 familiesA Elbaz, J Vale-Santos, K Jurkat-Rott, et al.
Human Molecular Genetics|August 1, 1994
A calcium channel mutation causing hypokalemic periodic paralysisK Jurkat-Rott, F Lehmann-Horn, A Elbaz, et al.
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