Utilizing multiple in silico analyses to identify putative causal SCN5A variants in Brugada syndrome.
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Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndromeJ-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledgeEnhanced Classification of Brugada Syndrome-Associated and Long-QT Syndrome-Associated Genetic Variants in the SCN5A-Encoded Na(v)1.5 Cardiac Sodium Channel.J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge.
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Utilizing multiple in silico analyses to identify putative causal SCN5A variants in Brugada syndrome.
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scientific article published on 27 January 2014
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name
Utilizing multiple in silico a ...... variants in Brugada syndrome.
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Utilizing multiple in silico a ...... variants in Brugada syndrome.
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type
label
Utilizing multiple in silico a ...... variants in Brugada syndrome.
@en
Utilizing multiple in silico a ...... variants in Brugada syndrome.
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prefLabel
Utilizing multiple in silico a ...... variants in Brugada syndrome.
@en
Utilizing multiple in silico a ...... variants in Brugada syndrome.
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P2093
P2860
P50
P356
P1433
P1476
Utilizing multiple in silico a ...... variants in Brugada syndrome.
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P2093
Chia-Hsiang Hsueh
Eric Y Chuang
Jiunn-Lee Lin
Sherri Shih-Fan Yeh
Yen-Bin Liu
P2860
P2888
P356
10.1038/SREP03850
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P50
P577
2014-01-27T00:00:00Z