Genetic modifiers to the PLN L39X mutation in a patient with DCM and sustained ventricular tachycardia?

about

Genetic modifiers to the PLN L39X mutation in a patient with DCM and sustained ventricular tachycardia?

Item

http://www.wikidata.org/entity/Q36187486

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

@zh

2015年论文

@zh-cn

name

Genetic modifiers to the PLN L ...... ained ventricular tachycardia?

@ast

Genetic modifiers to the PLN L ...... ained ventricular tachycardia?

@en

type

Item

label

Genetic modifiers to the PLN L ...... ained ventricular tachycardia?

@ast

Genetic modifiers to the PLN L ...... ained ventricular tachycardia?

@en

prefLabel

Genetic modifiers to the PLN L ...... ained ventricular tachycardia?

@ast

Genetic modifiers to the PLN L ...... ained ventricular tachycardia?

@en

P1476

Genetic modifiers to the PLN L ...... ained ventricular tachycardia?

@en

P2093

Dimitrios Kremastinos

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

Dimitris Tsiapras

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

Fotis Kolokathis

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

Kholoud Al-Shafai

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

Magdi Yacoub

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

Stuart A Cook

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

P2860

A role for Alström syndrome protein, alms1, in kidney ciliogenesis and cellular quiescence

The Ser96Ala variant in histidine-rich calcium-binding protein is associated with life-threatening ventricular arrhythmias in idiopathic dilated cardiomyopathy

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

The crystal structure of a laminin G-like module reveals the molecular basis of alpha-dystroglycan binding to laminins, perlecan, and agrin

Molecular heterogeneity of calcium channel beta-subunits in canine and human heart: evidence for differential subcellular localization

Cellular basis of triggered arrhythmias in heart failure

Phospholamban and cardiac contractile function.

Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death.

New concepts in hypertrophic cardiomyopathies, part I.

Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy

P304

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

P31

scholarly article

P356

10.5339/GCSP.2015.29

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

P433

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

P478

2015

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

P50

Roddy Walsh

Demetrios A. Arvanitis

Paul J Barton

Despina Sanoudou

Navaneethakrishnan T Krishnamoorthy

Rachel Buchan

P577

2015-07-03T00:00:00Z

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

P5875

277950295

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

P698

26535225

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

P932

4614339

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