Arrhythmogenesis in Timothy Syndrome is associated with defects in Ca2+-dependent inactivation-Reference-Cited by-同舟云学术

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Arrhythmogenesis in Timothy Syndrome is associated with defects in Ca2+-dependent inactivation

Published:2016-01-29 Issue:1 Volume:7 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

Dick Ivy E.,Joshi-Mukherjee Rosy,Yang Wanjun,Yue David T.

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

Link

http://www.nature.com/articles/ncomms10370.pdf

Reference61 articles.

1. Splawski, I. et al. Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations. Proc. Natl Acad. Sci. USA 102, 8089–8096 (2005) .

2. Splawski, I. et al. Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism. Cell 119, 19–31 (2004) .

3. Liao, P., Yong, T. F., Liang, M. C., Yue, D. T. & Soong, T. W. Splicing for alternative structures of Cav1.2 Ca2+ channels in cardiac and smooth muscles. Cardiovasc. Res. 68, 197–203 (2005) .

4. Liao, P. & Soong, T. W. CaV1.2 channelopathies: from arrhythmias to autism, bipolar disorder, and immunodeficiency. Pflugers Arch. 460, 353–359 (2010) .

5. Frohler, S. et al. Exome sequencing helped the fine diagnosis of two siblings afflicted with atypical Timothy syndrome (TS2). BMC Med. Genet. 15, 48 (2014) .

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