A case report of heterozygous familial hypercholesterolaemia with LDLR gene mutation complicated by premature coronary artery disease detected in primary care

由 Abdul-Halim M.A.Z.; Abdul-Hamid H.; Baharudin N.; Mohamed-Yassin M.-S.; Kasim S.S.; Nawawi H.; Qureshi N.; Ramli A.S.
發表在 European Heart Journal - Case Reports (2024)