参考文献/References:
[1] Abriel H, Zaklyazminskaya E V. Cardiac channelopathies: Genetic and molecular mechanisms [J]. Gene, 2013, 517(1): 1-11.
[2] Coronel R, Casini S, Koopmann T T, et al. Right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome—A combined electrophysiological, genetic, histopathologic, and computational study [J]. Circulation, 2005, 112(18): 2769-2777.
[3] Valdivia C R, Tester D J, Rok B A, et al. A trafficking defective, brugada syndrome-causing SCN5A in mutation rescued by drugs [J]. Cardiovascular Research, 2004, 62(1): 53-62.
[4] London B, Michalec M, Mehdi H, et al. Mutation in glycerol-3-phosphate dehydrogenase 1-like gene(GPD1-L)decreases cardiac Na+ current and causes inherited Arrhythmias [J]. Circulation, 2007, 116(20): 2260-2268.
[5] Nie Z, Hirsch D S, Randazzo PA. Arf and its many interactors [J]. Curr Opin Cell Biol, 2003, 15(4): 396-404.
[6] Stenmark H, Olkkonen V M. The Rab GTPase family [J]. Genome Biol, 2001, 2(5): Review,S3007.
[7] Amor J C, Harrison D H, Kahn R A, et al. Structure of the human ADP-ribosylation factor 1 complexed with GDP [J]. Nature, 1994, 372(6507): 704-708.
[8] Bednarek S Y, Ravazzola M, Hosobuchi M, et al. COPI- and COPII-coated vesicles bud directly from the endoplasmic reticulum in yeast [J]. Cell, 1995, 83(7): 1183-1196.
[9] Yoo J S, Moyer B D, Bannykh S, et al. Non-conventional trafficking of the cystic fibrosis transmembrane conductance regulator through the early secretory pathway [J]. Journal of Biological Chemistry, 2002, 277(13): 11401-11409.
[10] Delisle B P, Underkofler H A S, Moungey B M, et al. Small GTPase determinants for the golgi processing and plasmalemmal expression of human ether-a-go-go related(hERG)K+ channels [J]. Journal of Biological Chemistry, 2009, 284(5): 2844-2853.