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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1987 | 1 |
1994 | 1 |
1995 | 1 |
2024 | 0 |
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Dihydropyridine receptor mutations cause hypokalemic periodic paralysis.
Cell. 1994 Jun 17;77(6):863-8. doi: 10.1016/0092-8674(94)90135-x.
Cell. 1994.
PMID: 8004673
Primary structure of the receptor for calcium channel blockers from skeletal muscle.
Tanabe T, Takeshima H, Mikami A, Flockerzi V, Takahashi H, Kangawa K, Kojima M, Matsuo H, Hirose T, Numa S.
Tanabe T, et al.
Nature. 1987 Jul 23-29;328(6128):313-8. doi: 10.1038/328313a0.
Nature. 1987.
PMID: 3037387
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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.
Elbaz A, Vale-Santos J, Jurkat-Rott K, Lapie P, Ophoff RA, Bady B, Links TP, Piussan C, Vila A, Monnier N, et al.
Elbaz A, et al.
Am J Hum Genet. 1995 Feb;56(2):374-80.
Am J Hum Genet. 1995.
PMID: 7847370
Free PMC article.
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