M. Franco

Molecular characterization of familial hypercholesterolemia in Spain: Identification of 39 novel and 77 recurrent mutations in LDLR

M. Pocovi, R. Alonso, P. Mata, 2004, Human mutation.

Hyperlipoproteinaemia(a) is a common cause of autosomal dominant hypercholesterolaemia

E. Ros, F. Civeira, Á. Brea, 2007, Journal of Inherited Metabolic Disease.