Lone AF - Etiologic Factors and Genetic Insights into Pathophysiolgy.

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description

2010 nî lūn-bûn

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2010年の論文

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2010年学术文章

@wuu

2010年学术文章

@zh-cn

2010年学术文章

@zh-hans

2010年学术文章

@zh-my

2010年学术文章

@zh-sg

2010年學術文章

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2010年學術文章

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2010年學術文章

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name

Lone AF - Etiologic Factors and Genetic Insights into Pathophysiolgy.

@en

Lone AF - Etiologic Factors and Genetic Insights into Pathophysiolgy.

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type

Item

label

Lone AF - Etiologic Factors and Genetic Insights into Pathophysiolgy.

@en

Lone AF - Etiologic Factors and Genetic Insights into Pathophysiolgy.

@nl

prefLabel

Lone AF - Etiologic Factors and Genetic Insights into Pathophysiolgy.

@en

Lone AF - Etiologic Factors and Genetic Insights into Pathophysiolgy.

@nl

P1476

Lone AF - Etiologic Factors and Genetic Insights into Pathophysiolgy.

@en

P2093

Babar Parvez

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Dawood Darbar

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P2860

ACC/AHA/ESC 2006 Guidelines for the Management of Patients With Atrial Fibrillation

Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation

A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene

Novel KCNA5 loss-of-function mutations responsible for atrial fibrillation

Augmented potassium current is a shared phenotype for two genetic defects associated with familial atrial fibrillation

Mutation in nuclear pore component NUP155 leads to atrial fibrillation and early sudden cardiac death

KCNQ1 gain-of-function mutation in familial atrial fibrillation

Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation.

Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death

Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation

P304

236

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scholarly article

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10.4022/JAFIB.236

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P433

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P478

http://www.w3.org/2001/XMLSchema#string

P577

2010-06-01T00:00:00Z

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28496656

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5398815

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