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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1992 | 1 |
1993 | 2 |
1994 | 1 |
2024 | 0 |
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4 results
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Page 1
Functional consequences of a Na+ channel mutation causing hyperkalemic periodic paralysis.
Neuron. 1993 Apr;10(4):667-78. doi: 10.1016/0896-6273(93)90168-q.
Neuron. 1993.
PMID: 8386527
Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita.
Ptácek LJ, George AL Jr, Barchi RL, Griggs RC, Riggs JE, Robertson M, Leppert MF.
Ptácek LJ, et al.
Neuron. 1992 May;8(5):891-7. doi: 10.1016/0896-6273(92)90203-p.
Neuron. 1992.
PMID: 1316765
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Dihydropyridine receptor mutations cause hypokalemic periodic paralysis.
Ptácek LJ, Tawil R, Griggs RC, Engel AG, Layzer RB, Kwieciński H, McManis PG, Santiago L, Moore M, Fouad G, et al.
Ptácek LJ, et al.
Cell. 1994 Jun 17;77(6):863-8. doi: 10.1016/0092-8674(94)90135-x.
Cell. 1994.
PMID: 8004673
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Sodium channel mutations in paramyotonia congenita and hyperkalemic periodic paralysis.
Ptacek LJ, Gouw L, Kwieciński H, McManis P, Mendell JR, Barohn RJ, George AL Jr, Barchi RL, Robertson M, Leppert MF.
Ptacek LJ, et al.
Ann Neurol. 1993 Mar;33(3):300-7. doi: 10.1002/ana.410330312.
Ann Neurol. 1993.
PMID: 8388676
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