TY  - JOUR
AU  - Manuel, Ana Isabel Moreno
AU  - Gutiérrez, Lilian K
AU  - Pedrosa, María Linarejos Vera
AU  - Uréndez, Francisco Miguel Cruz
AU  - Jiménez, Francisco José Bermúdez
AU  - Carrascoso, Isabel Martínez
AU  - Pérez, Patricia Sánchez
AU  - Macías, Álvaro
AU  - Jalife, José
PY  - 2022
DO  - 10.1093/cvr/cvac118
UR  - http://hdl.handle.net/10668/19756
T2  - Cardiovascular research
AB  - Andersen Tawil Syndrome (ATS) is a rare inheritable disease associated with loss-of-function mutations in KCNJ2, the gene coding the strong inward rectifier potassium channel Kir2.1, which forms an essential membrane protein controlling cardiac...
LA  - en
KW  - KCNJ2 mutations
KW  - Kir2.1 mutations classification
KW  - Kir2.1-NaV1.5 channelosome
KW  - channelopathies
KW  - sarcoplasmic reticulum Kir2.1 channels
KW  - sudden cardiac death
TI  - Molecular stratification of arrhythmogenic mechanisms in the Andersen Tawil Syndrome.
TY  - research article
ER  -