Genetics and Genomics of Single-Gene Cardiovascular Diseases: Common Hereditary Cardiomyopathies as Prototypes of Single-Gene Disorders.

about

Dilated Cardiomyopathy: Genetic Determinants and Mechanisms.Molecular genetic diagnostics for ventricular arrhythmias and sudden cardiac death syndromes.Genetic Pathogenesis of Hypertrophic and Dilated Cardiomyopathy.Genetic Testing in Cardiovascular Medicine

P2860

Q50083275-51F887E4-DCE8-4379-8D0B-D112EF46A3BD Q52606226-DD5F80CB-08CB-4E5F-A752-3DE7BA18F489 Q52662539-F4AE2380-24BA-4A49-BD78-BF42AF061624 Q58130428-9EBF1DAB-162F-43BE-8922-53ECAC758572

P2860

Genetics and Genomics of Single-Gene Cardiovascular Diseases: Common Hereditary Cardiomyopathies as Prototypes of Single-Gene Disorders.

Item

http://www.wikidata.org/entity/Q39050554

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Genetics and Genomics of Singl ...... ypes of Single-Gene Disorders.

@en

Genetics and Genomics of Singl ...... ypes of Single-Gene Disorders.

@nl

type

Item

label

Genetics and Genomics of Singl ...... ypes of Single-Gene Disorders.

@en

Genetics and Genomics of Singl ...... ypes of Single-Gene Disorders.

@nl

prefLabel

Genetics and Genomics of Singl ...... ypes of Single-Gene Disorders.

@en

Genetics and Genomics of Singl ...... ypes of Single-Gene Disorders.

@nl

P1476

Genetics and Genomics of Singl ...... ypes of Single-Gene Disorders.

@en

P2093

Ali J Marian

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

Eva van Rooij

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

Robert Roberts

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

P2860

The diploid genome sequence of an Asian individual

Analysis of genetic inheritance in a family quartet by whole-genome sequencing

Mapping and sequencing of structural variation from eight human genomes

The complete genome of an individual by massively parallel DNA sequencing

Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis

Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy

Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy

Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing

P304

2831-2849

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

P31

scholarly article

P356

10.1016/J.JACC.2016.09.968

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

P407

English

P433

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

P478

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

P577

2016-12-01T00:00:00Z

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

P698

28007145

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

P921

cardiovascular disease

P932

5189923

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

Genetics and Genomics of Single-Gene Cardiovascular Diseases: Common Hereditary Cardiomyopathies as Prototypes of Single-Gene Disorders.

about

P2860

P2860

Genetics and Genomics of Single-Gene Cardiovascular Diseases: Common Hereditary Cardiomyopathies as Prototypes of Single-Gene Disorders.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P921

P932