(Q28264796)

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

scientific article

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

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Europe PubMed Central

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

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Andersen‐Tawil syndrome: a model of clinical variability, pleiotropy, and genetic heterogeneity (English)

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DOI.org query endpoint

https://doi.org/10.1080%2F17431380410032490

20 May 2017

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Andersen-Tawil syndrome

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author name string

Matthew R Donaldson

1

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Grace Yoon

2

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DOI.org query endpoint

https://doi.org/10.1080%2F17431380410032490

20 May 2017

Ying-Hui Fu

3

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Louis J Ptacek

4

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Matthew Donaldson

1

1 reference

DOI.org query endpoint

https://doi.org/10.1080%2F17431380410032490

20 May 2017

Ying‐Hui Fu

3

1 reference

DOI.org query endpoint

https://doi.org/10.1080%2F17431380410032490

20 May 2017

Louis Ptacek

4

1 reference

DOI.org query endpoint

https://doi.org/10.1080%2F17431380410032490

20 May 2017

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2004

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January 2004

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https://doi.org/10.1080%2F17431380410032490

20 May 2017

Annals of Medicine

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https://doi.org/10.1080%2F17431380410032490

20 May 2017

36 Suppl 1

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36

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https://doi.org/10.1080%2F17431380410032490

20 May 2017

sup1

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https://doi.org/10.1080%2F17431380410032490

20 May 2017

92-7

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92-97

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DOI.org query endpoint

https://doi.org/10.1080%2F17431380410032490

20 May 2017

Ion channel diseases

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032490

21 January 2018

Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032490

21 January 2018

Andersen's syndrome: A distinct periodic paralysis

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032490

21 January 2018

Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032490

21 January 2018

Function, subcellular localization and assembly of a novel mutation of KCNJ2 in Andersen's syndrome

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032490

21 January 2018

Regulation of cardiac inwardly rectifying potassium channels by membrane lipid metabolism

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032490

21 January 2018

Alterations in conserved Kir channel-PIP2 interactions underlie channelopathies

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032490

21 January 2018

The Structure of the Potassium Channel: Molecular Basis of K+ Conduction and Selectivity

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032490

21 January 2018

Inward rectifiers in the heart: an update on I(K1).

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032490

21 January 2018

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032490

21 January 2018

Targeting of an A kinase-anchoring protein, AKAP79, to an inwardly rectifying potassium channel, Kir2.1

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032490

21 January 2018

Targeting of PKA to glutamate receptors through a MAGUK-AKAP complex

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032490

21 January 2018

Murine CASK is disrupted in a sex-linked cleft palate mouse mutant

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032490

21 January 2018

Craniofacial dysmorphogenesis including cleft palate in mice with an insertional mutation in the discs large gene

1 reference

https://api.crossref.org/works/10.1080%2F17431380410032490

21 January 2018

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10.1080/17431380410032490

1 reference

DOI.org query endpoint

https://doi.org/10.1080%2F17431380410032490

20 May 2017

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