For citations:
Korneva V.A., Kuznetsova T.Yu., Bogoslovskaya T.Yu., Murtazina R.Z., Didio A.V., Serebrenitskaya M.P., Konstantinov V.O., Mandelshtam M.Yu., Vasiliev V.B. CLINICAL CASE OF A PATIENT WITH FAMILY HYPERCHOLESTEROLEMIA CAUSED BY MUTATION C.1859G>C (P.W620S) IN THE GENE OF HUMAN LOW DENSITY LIPOPROTEINS RECEPTOR. Cardiovascular Therapy and Prevention. 2015;14(6):52-53. (In Russ.) https://doi.org/10.15829/1728-8800-2015-6-52-53