TY  - JOUR
AU  - Amor-Salamanca, Almudena
AU  - Santana Rodríguez, Alfredo
AU  - Rasoul, Hazhee
AU  - Rodríguez-Palomares, José F
AU  - Moldovan, Oana
AU  - Hey, Thomas Morris
AU  - Delgado, María Gallego
AU  - Cuenca, David López
AU  - de Castro Campos, Daniel
AU  - Basurte-Elorz, María Teresa
AU  - Macías-Ruiz, Rosa
AU  - Fuentes Cañamero, María Eugenia
AU  - Galvin, Joseph
AU  - Bilbao Quesada, Raquel
AU  - de la Higuera Romero, Luis
AU  - Trujillo-Quintero, Juan Pablo
AU  - García-Cruz, Loida María
AU  - Cárdenas-Reyes, Ivonne
AU  - Jiménez-Jáimez, Juan
AU  - García-Hernández, Soledad
AU  - Valverde-Gómez, María
AU  - Gómez-Díaz, Iria
AU  - Limeres Freire, Javier
AU  - García-Pinilla, José M
AU  - Gimeno-Blanes, Juan R
AU  - Savattis, Konstantinos
AU  - Garcia-Pavia, Pablo
AU  - Ochoa, Juan Pablo
PY  - 2024
DO  - 10.1161/CIRCGEN.123.004404
UR  - http://hdl.handle.net/20.500.12105/20038
AB  - BACKGROUNDLess than 40% of patients with dilated cardiomyopathy (DCM) have a pathogenic/likely pathogenic genetic variant identified. TBX20 has been linked to congenital heart defects; although an association with left ventricular noncompaction (LVNC)...
LA  - eng
PB  - Lippincott Williams & Wilkins (LWW)
KW  - Cardiomyopathy, Dilated
KW  - Heart Defects, Congenital
KW  - Male
KW  - Humans
KW  - Adolescent
KW  - Young Adult
KW  - Adult
KW  - Middle Aged
KW  - Female
KW  - Arrhythmias, Cardiac
KW  - Phenotype
KW  - T-Box Domain Proteins
TI  - Role of TBX20 Truncating Variants in Dilated Cardiomyopathy and Left Ventricular Noncompaction.
TY  - journal article
ER  -