TY  - JOUR
AU  - Alonso, Rodrigo
AU  - Perez de Isla, Leopoldo
AU  - Muñiz-Grijalvo, Ovidio
AU  - Diaz-Diaz, Jose Luis
AU  - Mata, Pedro
PY  - 2018
DO  - 10.15420/ecr.2018:10:2
UR  - https://hdl.handle.net/10668/25880
T2  - European cardiology
AB  - Familial hypercholesterolaemia is the most common monogenic disorder associated with premature coronary artery disease. Mutations are most frequently found in the LDL receptor gene. Clinical criteria can be used to make the diagnosis; however, genetic...
LA  - en
KW  - Familial hypercholesterolaemia
KW  - cascade screening
KW  - genetic testing
KW  - statins
TI  - Familial Hypercholesterolaemia Diagnosis and Management.
TY  - research article
VL  - 13
ER  -