(Q28277370)

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Paramyotonia congenita: the R1448P Na+ channel mutation in adult human skeletal muscle

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title

Paramyotonia congenita: the R1448P Na+ channel mutation in adult human skeletal muscle (English)

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main subject

paramyotonia congenita

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H Lerche

1

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N Mitrovic

series ordinal

2

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V Dubowitz

series ordinal

3

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F Lehmann-Horn

series ordinal

4

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language of work or name

English

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publication date

May 1996

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published in

Annals of Neurology

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volume

39

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issue

5

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page(s)

599-608

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cites work

Human sodium channel myotonia: slowed channel inactivation due to substitutions for a glycine within the III-IV linker

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reference URL

https://api.crossref.org/works/10.1002%2FANA.410390509

retrieved

21 January 2018

K(+)-aggravated myotonia: destabilization of the inactivated state of the human muscle Na+ channel by the V1589M mutation

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FANA.410390509

retrieved

21 January 2018

Different effects on gating of three myotonia-causing mutations in the inactivation gate of the human muscle sodium channel

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FANA.410390509

retrieved

21 January 2018

Identifiers

DOI

10.1002/ANA.410390509

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PubMed ID

8619545

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ResearchGate publication ID

14580104

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(Q28277370)

Paramyotonia congenita: the R1448P Na+ channel mutation in adult human skeletal muscle

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