TY  - JOUR
AU  - Herraiz-Martínez, Adela
AU  - Llach, Anna
AU  - Tarifa, Carmen
AU  - Gandía, Jorge
AU  - Jiménez-Sabado, Verónica
AU  - Lozano-Velasco, Estefanía
AU  - Serra, Selma A
AU  - Vallmitjana, Alexander
AU  - Vázquez Ruiz de Castroviejo, Eduardo
AU  - Benítez, Raúl
AU  - Aranega, Amelia
AU  - Muñoz-Guijosa, Christian
AU  - Franco, Diego
AU  - Cinca, Juan
AU  - Hove-Madsen, Leif
PY  - 2019
DO  - 10.1093/cvr/cvy215
UR  - http://hdl.handle.net/10668/12952
T2  - Cardiovascular research
AB  - Single nucleotide polymorphisms on chromosome 4q25 have been associated with risk of atrial fibrillation (AF) but the exiguous knowledge of the mechanistic links between these risk variants and underlying electrophysiological alterations hampers their...
LA  - en
KW  - Human atrial myocytes
KW  - Ryanodine receptor
KW  - Sarcoplasmic reticulum calcium release
KW  - Single nucleotide polymorphisms
KW  - Spontaneous electrical activity
KW  - Action Potentials
KW  - Aged
KW  - Atrial Fibrillation
KW  - Calcium
KW  - Calcium Signaling
KW  - Case-Control Studies
KW  - Chromosomes, Human, Pair 4
KW  - Female
KW  - Genetic Association Studies
KW  - Genetic Predisposition to Disease
KW  - Heart Atria
KW  - Heart Rate
KW  - Homeostasis
KW  - Humans
KW  - Male
KW  - Myocytes, Cardiac
KW  - Phenotype
KW  - Phosphorylation
KW  - Polymorphism, Single Nucleotide
KW  - Risk Factors
KW  - Ryanodine Receptor Calcium Release Channel
KW  - Sarcoplasmic Reticulum Calcium-Transporting ATPases
TI  - The 4q25 variant rs13143308T links risk of atrial fibrillation to defective calcium homoeostasis.
TY  - research article
VL  - 115
ER  -