Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation

OBJECTIVES: This study tested the hypothesis that two common polymorphisms in the chromosome 4q25 region that have been associated with atrial fibrillation (AF) contribute to the variable penetrance of familial AF. BACKGROUND: Although mutations in ion channels, gap junction proteins, and signaling...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Ritchie, Marylyn D, Rowan, Shane, Kucera, Gayle, Stubblefield, Tanya, Blair, Marcia, Roden, Dan M, Darbar, Dawood
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2012
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3448817/
https://ncbi.nlm.nih.gov/pubmed/22818067
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jacc.2012.04.030
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