Fifteen Genetic Loci Associated With the Electrocardiographic P Wave.

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PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval

P2860

Q57258977-135AD56C-3BE7-4E78-B0D1-85289F769D6C Q57258989-57D2A3E9-FE4C-48AB-9CEA-35923C5B0FB3

P2860

Fifteen Genetic Loci Associated With the Electrocardiographic P Wave.

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http://www.wikidata.org/entity/Q38644720

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

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2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

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2017年學術文章

@zh-hant

name

Fifteen Genetic Loci Associated With the Electrocardiographic P Wave.

@en

type

Item

label

Fifteen Genetic Loci Associated With the Electrocardiographic P Wave.

@en

prefLabel

Fifteen Genetic Loci Associated With the Electrocardiographic P Wave.

@en

P1476

Fifteen Genetic Loci Associated With the Electrocardiographic P Wave.

@en

P2093

Aaron Isaacs

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

Alex P Reiner

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

Alexander Teumer

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

Andre Uitterlinden

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

Astrid Petersmann

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

Bouwe P Krijthe

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

Bruno H Stricker

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

Christian Müller

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

Christy L Avery

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

Dan E Arking

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

P2860

Cardiac alpha-myosin (MYH6) is the predominant sarcomeric disease gene for familial atrial septal defects

Genetic variation in SCN10A influences cardiac conduction

Mutation in myosin heavy chain 6 causes atrial septal defect

Alpha-myosin heavy chain: a sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy

Genome-wide association analysis identifies multiple loci related to resting heart rate

PLINK: a tool set for whole-genome association and population-based linkage analyses

Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy

Alpha-cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

Common genetic variation near the connexin-43 gene is associated with resting heart rate in African Americans: a genome-wide association study of 13,372 participants.

P31

scholarly article

meta-analysis

P356

10.1161/CIRCGENETICS.116.001667

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

P433

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

P478

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

P50

Cornelia M. van Duijn

Emelia J. Benjamin

Martina Müller-Nurasyid

Ingrid Christophersen

Jan A Kors

Marcus Dörr

P577

2017-08-01T00:00:00Z

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

P698

28794112

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

P921

electrocardiography

P932

5567993

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

Fifteen Genetic Loci Associated With the Electrocardiographic P Wave.

about

P2860

P2860

Fifteen Genetic Loci Associated With the Electrocardiographic P Wave.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P31

P356

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P31

P356

P433

P478

P50

P577

P698

P921

P932