TY  - JOUR 
AU  - Allegue, C.
AU  - Coll, M.
AU  - Mates, J.
AU  - Campuzano, O.
AU  - Iglesias, A.
AU  - Sobrino Rey, Beatríz
AU  - Brión Martínez, María José
AU  - Amigo Lechuga, Jorge
AU  - Carracedo Álvarez, Ángel
AU  - Brugada, P.
AU  - Brugada, J.
AU  - Brugada, R.
PY  - 2015
SN  - 1932-6203
UR  - http://hdl.handle.net/20.500.11940/1467
AB  - BACKGROUND: The use of next-generation sequencing enables a rapid analysis of many genes associated with sudden cardiac death in diseases like Brugada Syndrome. Genetic variation is identified and associated with 30-35% of cases of Brugada Syndrome,...
LA  - eng
KW  - A Kinase Anchor Proteins
KW  - Adult
KW  - Ankyrins
KW  - Arrhythmias, Cardiac
KW  - Brugada Syndrome
KW  - Calsequestrin
KW  - Clinical Decision-Making
KW  - Cohort Studies
KW  - Cytoskeletal Proteins
KW  - Death, Sudden, Cardiac
KW  - Desmoglein 2
KW  - Desmoplakins
KW  - Female
KW  - Genetic Testing
KW  - Genetic Variation
KW  - High-Throughput Nucleotide Sequencing
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - NAV1.5 Voltage-Gated Sodium Channel
KW  - Pedigree
KW  - Penetrance
KW  - Potassium Channels, Inwardly Rectifying
KW  - Retrospective Studies
KW  - Ryanodine Receptor Calcium Release Channel
KW  - Sequence Analysis, DNA
KW  - gamma Catenin
TI  - Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome
DO  - 10.1371/journal.pone.0133037
T2  - PLoS One
M2  - e0133037
VL  - 10
ER  -