Brugada syndrome and calcium channel mutation in a patient with congenital deaf mutism.

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Brugada syndrome and calcium channel mutation in a patient with congenital deaf mutism.

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

@yue

2017年論文

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2017年論文

@zh-hk

2017年論文

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2017年論文

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2017年论文

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2017年论文

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2017年论文

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Brugada syndrome and calcium channel mutation in a patient with congenital deaf mutism.

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Brugada syndrome and calcium channel mutation in a patient with congenital deaf mutism.

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Brugada syndrome and calcium channel mutation in a patient with congenital deaf mutism.

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P1476

Brugada syndrome and calcium channel mutation in a patient with congenital deaf mutism

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P2093

Cem Coteli

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Kudret Aytemir

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P2860

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

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death.

What can naturally occurring mutations tell us about Ca(v)1.x channel function?

HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013.

Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma.

Brugada Syndrome Unmasked by Heat Exhaustion.

P304

16-17

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scholarly article

case report

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10.1016/J.IPEJ.2017.01.002

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P407

English

P433

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P478

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P50

Ugur Canpolat

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2017-01-09T00:00:00Z

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P698

28401855

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P921

birth defect

P932

5357834

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