The pathology of complete atrio-ventricular block, Prog Cardiovas Dis, vol.6, pp.317-340, 1964. ,
Anatomic basis for atrioventricular block, The American Journal of Medicine, vol.37, issue.5, pp.742-750, 1964. ,
DOI : 10.1016/0002-9343(64)90022-1
Pathology of chronic AV block, Acta Cardiol, vol.21, pp.19-30, 1976. ,
Familial bundle branch block, American Heart Journal, vol.64, issue.3, pp.397-400, 1962. ,
DOI : 10.1016/0002-8703(62)90156-4
Gene for Progressive Familial Heart Block Type I Maps to Chromosome 19q13, Circulation, vol.91, issue.6, pp.1633-1673, 1995. ,
DOI : 10.1161/01.CIR.91.6.1633
Congenital arrhythmias and conduction abnormalities in a father and four children, Can Med Assoc J, vol.84, pp.1283-96, 1961. ,
Four cases of ???benign??? left bundle branch block in the same family, American Heart Journal, vol.51, issue.3, pp.398-404, 1956. ,
DOI : 10.1016/0002-8703(56)90065-5
A survey of familial heart block., Heart, vol.36, issue.7, pp.693-699, 1974. ,
DOI : 10.1136/hrt.36.7.693
The Genetic Origin of Atrioventricular Conduction Disturbance in Humans, Novartis Found Symp, vol.250, pp.242-52, 2003. ,
DOI : 10.1002/0470868066.ch15
An Isolated Cardiac Conduction Disease Maps to Chromosome 19q, Circulation Research, vol.77, issue.4, pp.735-775, 1995. ,
DOI : 10.1161/01.RES.77.4.735
Hereditary bundle branch defect: Right bundle branch blocks of different causes have different morphologic characteristics, American Heart Journal, vol.133, issue.2, pp.249-56, 1997. ,
DOI : 10.1016/S0002-8703(97)70215-1
Cardiac conduction defects associate with mutations in SCN5A, Nature Genetics, vol.23, issue.1, pp.20-21, 1999. ,
DOI : 10.1038/12618
Sodium channel beta1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans, J Clin Invest, vol.118, pp.2260-2268, 2008. ,
DOI : 10.1172/jci33891
URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2373423/pdf
Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type I, Journal of Clinical Investigation, vol.119, issue.9, pp.2737-2781, 2009. ,
DOI : 10.1172/JCI38292DS1
Gain-of-Function Mutations in TRPM4 Cause Autosomal Dominant Isolated Cardiac Conduction Disease, Circulation: Cardiovascular Genetics, vol.3, issue.4, pp.374-85, 2010. ,
DOI : 10.1161/CIRCGENETICS.109.930867
Familial Aggregation of Calcific Aortic Valve Stenosis in the Western Part of France, Circulation, vol.113, issue.6, pp.856-60, 2006. ,
DOI : 10.1161/CIRCULATIONAHA.105.569467
AHA/ACCF/HRS Recommendations for the Standardization and Interpretation of the Electrocardiogram: Part III: Intraventricular Conduction Disturbances: A Scientific Statement From the American Heart Association Electrocardiography and Arrhythmias Committee, Council on Clinical Cardiology; the American College of Cardiology Foundation; and the Heart Rhythm Society: Endorsed by the International Society for Computerized Electrocardiology, Circulation, vol.119, issue.10, pp.235-275, 2009. ,
DOI : 10.1161/CIRCULATIONAHA.108.191095
Hemiblocks Revisited, Circulation, vol.115, issue.9, pp.1154-63, 2007. ,
DOI : 10.1161/CIRCULATIONAHA.106.637389
URL : http://circ.ahajournals.org/content/circulationaha/115/9/1154.full.pdf
Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Len??gre disease, Journal of the American College of Cardiology, vol.41, issue.4, pp.643-52, 2003. ,
DOI : 10.1016/S0735-1097(02)02864-4
Chronic Bifascicular Block: Evaluation of Familial Factors, Annals of Internal Medicine, vol.84, issue.5, pp.521-526, 1976. ,
DOI : 10.7326/0003-4819-84-5-521
Familial fascicular block: Histologic features of Lev's disease, American Heart Journal, vol.109, issue.6, pp.1399-401, 1985. ,
DOI : 10.1016/0002-8703(85)90377-1
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction, Nature Genetics, vol.16, issue.12, pp.1068-76, 2010. ,
DOI : 10.1073/pnas.95.19.11371
URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3338195/pdf
Genetic Determinants of Cardiac (Electric) Conduction, Circulation Research, vol.108, issue.4, pp.402-405, 2011. ,
DOI : 10.1161/RES.0b013e31821255f8
URL : http://circres.ahajournals.org/content/circresaha/108/4/402.full.pdf
Genetic variation in SCN10A influences cardiac conduction, Nature Genetics, vol.103, issue.2, pp.149-52, 2010. ,
DOI : 10.1038/nature05880
Several common variants modulate heart rate, PR interval and QRS duration, Nature Genetics, vol.37, issue.2, pp.117-139, 2010. ,
DOI : 10.1161/01.CIR.5.5.693
Genome-Wide Association Studies of the PR Interval in African Americans, PLoS Genetics, vol.5, issue.2, p.1001304, 2010. ,
DOI : 10.1371/journal.pgen.1001304.s006
Genome-wide association study of PR interval, Nature Genetics, vol.81, issue.2, pp.153-162, 2010. ,
DOI : 10.1002/ar.a.20102