Diagnosis of skeletal muscle channelopathies (Q38143226)

29 August 2017

title

Diagnosis of skeletal muscle channelopathies (English)

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29 August 2017

1

Jennifer Spillane

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29 August 2017

Doreen Fialho

2

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29 August 2017

Michael G Hanna

series ordinal

3

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29 August 2017

language of work or name

English

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publication date

26 September 2013

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Expert Opinion on Medical Diagnostics

29 August 2017

published in

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29 August 2017

volume

7

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29 August 2017

issue

6

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29 August 2017

page(s)

517-529

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Prevalence study of genetically defined skeletal muscle channelopathies in England

29 August 2017

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KCNJ2 mutation results in Andersen syndrome with sex-specific cardiac and skeletal muscle phenotypes

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Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis

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Cold induces shifts of voltage dependence in mutant SCN4A, causing hypokalemic periodic paralysis

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17530059.2013.839656

Andersen-Tawil syndrome: a model of clinical variability, pleiotropy, and genetic heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17530059.2013.839656

Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17530059.2013.839656

An algorithm for candidate sequencing in non-dystrophic skeletal muscle channelopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F17530059.2013.839656

10.1517/17530059.2013.839656

21 January 2018

Identifiers

DOI

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29 August 2017

1 reference