Allelic Complexity in Long QT Syndrome: A Family-Case Study.

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Allelic Complexity in Long QT Syndrome: A Family-Case Study.

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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年學術文章

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Allelic Complexity in Long QT Syndrome: A Family-Case Study.

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Allelic Complexity in Long QT Syndrome: A Family-Case Study.

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Allelic Complexity in Long QT Syndrome: A Family-Case Study.

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P1476

Allelic Complexity in Long QT Syndrome: A Family-Case Study

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P2093

Alberto Zullo

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Alfred L George

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Carlos G Vanoye

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Emanuele Romeo

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Nicola Detta

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Raffaele Calabrò

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P2860

Rescue of aberrant gating by a genetically encoded PAS (Per-Arnt-Sim) domain in several long QT syndrome mutant human ether-á-go-go-related gene potassium channels

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test

The multi-faceted aspects of the complex cardiac Nav1.5 protein in membrane function and pathophysiology

Analysis of protein-coding genetic variation in 60,706 humans

Determinants of incomplete penetrance and variable expressivity in heritable cardiac arrhythmia syndromes

Structural properties of PAS domains from the KCNH potassium channels

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects

Human Cystathionine-β-Synthase Phosphorylation on Serine227 Modulates Hydrogen Sulfide Production in Human Urothelium

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scholarly article

P356

10.3390/IJMS18081633

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P407

English

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P478

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P50

P577

2017-07-27T00:00:00Z

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P698

28749435

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P932

5578023

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