"Finnish" mutations in LDL receptor gene: a rare cause of familial hypercholesterolemia in St. Petersburg and Petrozavodsk.

Autor: Komarova TY; Institute of Experimental Medicine, North-Western Division of the Russian Academy of Medical Sciences, St. Petersburg, Russia. michail@MM13666.spb.edu., Golovina AS, Grudinina NA, Zakharova FM, Korneva VA, Lipovetskii BM, Serebrenitskaya MP, Konstantinov VO, Vasilyev VB, Mandelshtam MY

Publikováno v: Bulletin of experimental biology and medicine [Bull Exp Biol Med] 2013 Jul; Vol. 155 (3), pp. 380-3.