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1.Syndactyly and long QT syndrome (CaV1.2 missense mutation G406R) is associated with hypertrophic cardiomyopathy.

Lo-A-Njoe SM, Wilde AA, van Erven L, Blom NA.
Heart Rhythm. 2005 Dec;2(12):1365-8.
2. Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism.
Splawski I, Timothy KW, Sharpe LM, et al.
Cell 2004 Oct 1; 119(1):19-31.

实在是文献检索学的不怎么样啊，哈哈，又得找大家帮忙！
谢谢！

[ 此帖被诸葛笨笨在2009-03-26 10:56重新编辑 ]