Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2.
about
Role of risk stratification and genetics in sudden cardiac death.Combined gating and trafficking defect in Kv11.1 manifests as a malignant long QT syndrome phenotype in a large Danish p.F29L founder family.MicroRNAs in cardiac arrhythmia: DNA sequence variation of MiR-1 and MiR-133A in long QT syndromeRe-evaluating pathogenicity of variants associated with the long QT syndrome.
P2860
Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2.
description
2014 nî lūn-bûn
@nan
2014 թուականի Մարտին հրատարակուած գիտական յօդուած
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2014 թվականի մարտին հրատարակված գիտական հոդված
@hy
2014年の論文
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2014年論文
@yue
2014年論文
@zh-hant
2014年論文
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2014年論文
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2014年論文
@zh-tw
2014年论文
@wuu
name
Mutations in Danish patients w ...... r family with p.F29L in KCNH2.
@ast
Mutations in Danish patients w ...... r family with p.F29L in KCNH2.
@en
type
label
Mutations in Danish patients w ...... r family with p.F29L in KCNH2.
@ast
Mutations in Danish patients w ...... r family with p.F29L in KCNH2.
@en
prefLabel
Mutations in Danish patients w ...... r family with p.F29L in KCNH2.
@ast
Mutations in Danish patients w ...... r family with p.F29L in KCNH2.
@en
P2093
P2860
P50
P356
P1433
P1476
Mutations in Danish patients w ...... r family with p.F29L in KCNH2.
@en
P2093
Birgitte Stoevring
Finn L Henriksen
Frederik H Aidt
Jim Hansen
Jørgen K Kanters
Karina M Sørensen
Lisbeth N Pedersen
Michael Christiansen
Michael G Hansen
P2860
P2888
P356
10.1186/1471-2350-15-31
P50
P577
2014-03-07T00:00:00Z
P5875
P6179
1008157375