TY  - JOUR
AU  - Mates, Jesus
AU  - Mademont-Soler, Irene
AU  - Del Olmo, Bernat
AU  - Ferrer-Costa, Carles
AU  - Coll, Monica
AU  - Pérez-Serra, Alexandra
AU  - Picó, Ferran
AU  - Allegue, Catarina
AU  - Fernandez-Falgueras, Anna
AU  - Álvarez, Patricia
AU  - Yotti, Raquel
AU  - Espinosa, Maria Angeles
AU  - Sarquella-Brugada, Georgia
AU  - Cesar, Sergi
AU  - Carro, Ester
AU  - Brugada, Josep
AU  - Arbelo, Elena
AU  - Garcia-Pavia, Pablo
AU  - Borregan, Mar
AU  - Tizzano, Eduardo
AU  - López-Granados, Amador
AU  - Mazuelos, Francisco
AU  - Díaz de Bustamante, Aranzazu
AU  - Darnaude, Maria Teresa
AU  - González-Hevia, José Ignacio
AU  - Díaz-Flores, Felícitas
AU  - Trujillo, Francisco
AU  - Iglesias, Anna
AU  - Fernandez-Aviles, Francisco
AU  - Campuzano, Oscar
AU  - Brugada, Ramon
PY  - 2018
DO  - 10.1038/s41431-018-0119-1
UR  - http://hdl.handle.net/10668/12213
T2  - European journal of human genetics : EJHG
AB  - Several studies have identified copy number variants (CNVs) as responsible for cardiac diseases associated with sudden cardiac death (SCD), but very few exhaustive analyses in large cohorts of patients have been performed, and they have been generally...
LA  - en
KW  - Adult
KW  - Arrhythmias, Cardiac
KW  - Autopsy
KW  - Cardiomyopathies
KW  - DNA Copy Number Variations
KW  - Death, Sudden, Cardiac
KW  - Female
KW  - Genetic Testing
KW  - Heart
KW  - High-Throughput Nucleotide Sequencing
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - Phenotype
TI  - Role of copy number variants in sudden cardiac death and related diseases: genetic analysis and translation into clinical practice.
TY  - research article
VL  - 26
ER  -