Author:
Grau Isel,Sengupta Dipankar,Farid Dewan Md.,Manderick Bernard,Nowe Ann,Garcia Lorenzo Maria M.,Daneels Dorien,Bonduelle Maryse,Croes Didier,Van Dooren Sonia
Publisher
Springer International Publishing
Reference17 articles.
1. Saunders, C.J., et al.: Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units. Sci. Transl. Med. 4, 135–154 (2012)
2. Hofman, N., et al.: Yield of molecular and clinical testing for arrhythmia syndromes: report of a 15 years’ experience. Circulation 1513–1521 (2013)
3. Schulze-Bahr, E., et al.: Molecular genetics of arrhythmias – a new paradigm. Z Kardiol. 89(4), IV12–IV22 (2000)
4. Wilde, A.A.M., Tan, H.L.: Inherited arrhythmia syndromes. Circ. J. 71(Supplement A), A12–A19 (2007)
5. Stenson, P.D., et al.: Human gene mutation database HGMD: 2003 update. Hum. Mutat. 21(6), 577–581 (2003)