Sudden Infant Death Syndrome in Mice with an Inherited Mutation in RyR2

BACKGROUND: Mutations in the cardiac ryanodine receptor gene (RYR2) have been recently identified in victims of sudden infant death syndrome (SIDS). The aim of this study was to determine whether a gain-of-function mutation in RYR2 increases the propensity to cardiac arrhythmias and sudden death in...

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Detalhes bibliográficos
Main Authors: Mathur, Nitin, Sood, Subeena, Wang, Sufen, van Oort, Ralph J., Sarma, Satyam, Li, Na, Skapura, Darlene G., Bayle, J. Henri, Valderrábano, Miguel, Wehrens, Xander H.T.
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2796595/
https://ncbi.nlm.nih.gov/pubmed/20009080
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCEP.109.894683
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