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

Sudden infant death syndrome (SIDS) is the most frequent manner of post-perinatal death among infants. One of the suggested causes of the syndrome is inherited cardiac diseases, mainly channelopathies, that can trigger arrhythmias and sudden death. The purpose of this study was to investigate cases...

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Bibliografiska uppgifter
I publikationen:Eur J Hum Genet
Huvudupphovsmän: 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
Materialtyp: Artigo
Språk:Inglês
Publicerad: Nature Publishing Group 2016
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4867441/
https://ncbi.nlm.nih.gov/pubmed/26350513
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2015.198
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