Connexin43 Mutation Causes Heterogeneous Gap Junction Loss and Sudden Infant Death

BACKGROUND: An estimated 10-15% of sudden infant death syndrome (SIDS) may stem from channelopathy-mediated lethal arrhythmias. Loss of the GJA1-encoded gap junction channel protein connexin43 (Cx43) is known to underlie formation of lethal arrhythmias. GJA1 mutations have been associated with cardi...

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Detaylı Bibliyografya
Asıl Yazarlar: Van Norstrand, David W., Asimaki, Angeliki, Rubinos, Clio, Dolmatova, Elena, Srinivas, Miduturu, Tester, David J., Saffitz, Jeffrey E., Duffy, Heather S., Ackerman, Michael J.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2011
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Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3332541/
https://ncbi.nlm.nih.gov/pubmed/22179534
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCULATIONAHA.111.057224
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