Genetic investigations of sudden unexpected deaths in infancy using next-generation sequencing of 100 genes associated with cardiac diseases-Reference-Cited by-同舟云学术

Genetic investigations of sudden unexpected deaths in infancy using next-generation sequencing of 100 genes associated with cardiac diseases

Published:2015-09-09 Issue:6 Volume:24 Page:817-822
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Hertz Christin Loeth,Christiansen Sofie Lindgren,Larsen Maiken Kudahl,Dahl Morten,Ferrero-Miliani Laura,Weeke Peter Ejvin,Pedersen Oluf,Hansen Torben,Grarup Niels,Ottesen Gyda Lolk,Frank-Hansen Rune,Banner Jytte,Morling Niels

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

https://www.nature.com/articles/ejhg2015198.pdf

Reference48 articles.

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3. Moon RY, Horne RS, Hauck FR : Sudden infant death syndrome. Lancet 2007; 370: 1578–1587.

4. Winkel BG, Holst AG, Theilade J et al: Sudden unexpected death in infancy in Denmark. Scand Cardiovasc J 2011; 45: 14–20.

5. Millat G, Kugener B, Chevalier P et al: Contribution of long-QT syndrome genetic variants in sudden infant death syndrome. Pediatr Cardiol 2009; 30: 502–509.

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