遺伝子に刻まれた旅の記憶
Author:
Affiliation:
1. National Cerebral and Cardiovascular Center
Publisher
The Japanese Society of Electrocardiology
Subject
Pharmacology (medical)
Link
https://www.jstage.jst.go.jp/article/jse/42/4/42_201/_pdf
Reference5 articles.
1. 1) . Ahmad F, Li D, Karibe A, et al. : Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23. Circulation, 1998 ; 98 : 2791-2795
2. 2) . Merner ND, Hodgkinson KA, Haywood AF, et al. : Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene. Am J Hum Genet, 2008 ; 82 : 809-821
3. 3) . Milting H, Klauke B, Christensen AH, et al. : The TMEM43 Newfoundland mutation p.S358L causing ARVC-5 was imported from Europe and increases the stiffness of the cell nucleus. Eur Heart J, 2015 ; 36 : 872-881
4. 4) . Winbo A, Diamant UB, Rydberg A, et al. : Origin of the Swedish long QT syndrome Y111C/KCNQ1 founder mutation. Heart Rhythm, 2011 ; 8 : 541-547
5. 5) . Takahashi K, Shimizu W, Miyake A, et al. : High prevalence of the SCN5A E1784K mutation in school children with long QT syndrome living on the Okinawa islands. Circ J, 2014 ; 78 : 1974-1979
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