A new variant (c.1A>G)in LDLRAP1 causing autosomal recessive hypercholesterolemia: Characterization of the defect and response to PCSK9 inhibition

1. Rodríguez-Jiménez, C.
2. Gómez-Coronado, D.
3. Frías Vargas, M.
4. Cerrato, F.
5. Lahoz, C.
6. Saban-Ruiz, J.
7. González-Nieto, D.
8. Lasunción, M.A.
9. Mostaza, J.M.
10. Rodríguez-Nóvoa, S.