Mechanisms of a human skeletal myotonia produced by mutation in the C-terminus of NaV1.4: is Ca2+ regulation defective? (Q35063865)

6 August 2017

title

Mechanisms of a human skeletal myotonia produced by mutation in the C-terminus of NaV1.4: is Ca2+ regulation defective? (English)

1 reference

6 August 2017

Subrata Biswas

1

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6 August 2017

Deborah A DiSilvestre

series ordinal

2

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6 August 2017

Peihong Dong

series ordinal

3

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6 August 2017

Gordon F Tomaselli

series ordinal

4

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6 August 2017

language of work or name

English

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publication date

6 December 2013

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6 August 2017

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6 August 2017

volume

8

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6 August 2017

issue

12

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6 August 2017

page(s)

e81063

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Creative Commons Attribution 3.0 Unported

6 August 2017

copyright license

start time

6 December 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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12 December 2020

Secondary structure of the human cardiac Na+ channel C terminus: evidence for a role of helical structures in modulation of channel inactivation

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12 December 2020

A defect in skeletal muscle sodium channel deactivation exacerbates hyperexcitability in human paramyotonia congenita

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A large German kindred with cold-aggravated myotonia and a heterozygous A1481D mutation in the SCN4A gene

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10.1371/JOURNAL.PONE.0081063

Identifiers

DOI

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6 August 2017

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6 August 2017

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