Massively Parallel Sequencing of Genes Implicated in Heritable Cardiac Disorders: A Strategy for a Small Diagnostic Laboratory.

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Massively Parallel Sequencing of Genes Implicated in Heritable Cardiac Disorders: A Strategy for a Small Diagnostic Laboratory.

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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

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Massively Parallel Sequencing ...... a Small Diagnostic Laboratory.

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Massively Parallel Sequencing ...... a Small Diagnostic Laboratory.

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Massively Parallel Sequencing ...... a Small Diagnostic Laboratory.

@en

Massively Parallel Sequencing ...... a Small Diagnostic Laboratory.

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Massively Parallel Sequencing ...... a Small Diagnostic Laboratory.

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Massively Parallel Sequencing ...... a Small Diagnostic Laboratory.

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P1476

Massively Parallel Sequencing ...... a Small Diagnostic Laboratory

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P2093

Alexander Stuckey

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Daniele Belluoccio

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Debra O Prosser

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Donald R Love

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Jonathan R Skinner

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Vicky Fan

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P2860

Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome

Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular 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 Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance

A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel

The genetic basis of long QT and short QT syndromes: a mutation update

Next-generation DNA sequencing methods

Clinical and genetic characterization of families with arrhythmogenic right ventricular dysplasia/cardiomyopathy provides novel insights into patterns of disease expression

Clinical features of arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in plakophilin-2

Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy

P31

scholarly article

P356

10.3390/MEDSCI5040022

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P433

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P478

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P50

Ivone U S Leong

P577

2017-10-10T00:00:00Z

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P698

29099038

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P932

5753651

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