(Q43736265)

26 November 2017

title

Muscle weakness in a Japanese family of Arg1239His mutation hypokalemic periodic paralysis (English)

1 reference

26 November 2017

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Kusumi M

1

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26 November 2017

Kumada H

series ordinal

2

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26 November 2017

Adachi Y

series ordinal

3

1 reference

26 November 2017

Nakashima K

series ordinal

4

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26 November 2017

publication date

1 October 2001

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Psychiatry and Clinical Neurosciences

26 November 2017

published in

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26 November 2017

volume

55

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26 November 2017

issue

5

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26 November 2017

page(s)

539-541

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A calcium channel mutation causing hypokalemic periodic paralysis

26 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1819.2001.00902.X

Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1819.2001.00902.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1819.2001.00902.X

Identification of mutations in the CACNL1A3 gene in 13 families of Scandinavian origin having hypokalemic periodic paralysis and evidence of a founder effect in Danish families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1819.2001.00902.X

Familial hypokalaemic periodic paralysis in Finland

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1819.2001.00902.X

Structure and function of voltage-sensitive ion channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1440-1819.2001.00902.X

10.1046/J.1440-1819.2001.00902.X

21 January 2018

Identifiers

DOI

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26 November 2017

1 reference