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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 by V. A. Korneva, T. Yu. Kuznetsova, T. Yu. Bogoslovskaya, R. Z. Murtazina, A. V. Didio, M. P. Serebrenitskaya, V. O. Konstantinov, M. Yu. Mandelshtam, V. B. Vasiliev
Published 2015-12-01
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