Кардиоваскулярная терапия и профилактика (Dec 2015)
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
Abstract
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.