Multiple splicing defects caused by hERG splice site mutation 2592+1G>A associated with long QT syndrome.
about
Translational toxicology and rescue strategies of the hERG channel dysfunction: biochemical and molecular mechanistic aspectsIsoform-specific dominant-negative effects associated with hERG1 G628S mutation in long QT syndrome.LQT2 nonsense mutations generate trafficking defective NH2-terminally truncated channels by the reinitiation of translation.Early LQT2 nonsense mutation generates N-terminally truncated hERG channels with altered gating properties by the reinitiation of translation.
P2860
Multiple splicing defects caused by hERG splice site mutation 2592+1G>A associated with long QT syndrome.
description
2010 nî lūn-bûn
@nan
2010 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Multiple splicing defects caus ...... ociated with long QT syndrome.
@ast
Multiple splicing defects caus ...... ociated with long QT syndrome.
@en
Multiple splicing defects caus ...... ociated with long QT syndrome.
@nl
type
label
Multiple splicing defects caus ...... ociated with long QT syndrome.
@ast
Multiple splicing defects caus ...... ociated with long QT syndrome.
@en
Multiple splicing defects caus ...... ociated with long QT syndrome.
@nl
prefLabel
Multiple splicing defects caus ...... ociated with long QT syndrome.
@ast
Multiple splicing defects caus ...... ociated with long QT syndrome.
@en
Multiple splicing defects caus ...... ociated with long QT syndrome.
@nl
P2093
P2860
P1476
Multiple splicing defects caus ...... ociated with long QT syndrome.
@en
P2093
Matthew R Stump
Qiuming Gong
Zhengfeng Zhou
P2860
P304
P356
10.1152/AJPHEART.00818.2010
P577
2010-11-05T00:00:00Z