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

  • 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

DOI
https://doi.org/10.15829/1728-8800-2015-6-52-53
Journal volume & issue
Vol. 14, no. 6
pp. 52 – 53

Abstract

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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.