Ontology highlight
ABSTRACT:
SUBMITTER: Hopkins PN
PROVIDER: S-EPMC5098466 | biostudies-literature | 2015 Dec
REPOSITORIES: biostudies-literature
Hopkins Paul N PN Defesche Joep J Fouchier Sigrid W SW Bruckert Eric E Luc Gérald G Cariou Bertrand B Sjouke Barbara B Leren Trond P TP Harada-Shiba Mariko M Mabuchi Hiroshi H Rabès Jean-Pierre JP Carrié Alain A van Heyningen Charles C Carreau Valérie V Farnier Michel M Teoh Yee P YP Bourbon Mafalda M Kawashiri Masa-Aki MA Nohara Atsushi A Soran Handrean H Marais A David AD Tada Hayato H Abifadel Marianne M Boileau Catherine C Chanu Bernard B Katsuda Shoji S Kishimoto Ichiro I Lambert Gilles G Makino Hisashi H Miyamoto Yoshihiro Y Pichelin Matthieu M Yagi Kunimasa K Yamagishi Masakazu M Zair Yassine Y Mellis Scott S Yancopoulos George D GD Stahl Neil N Mendoza Johanna J Du Yunling Y Hamon Sara S Krempf Michel M Swergold Gary D GD
Circulation. Cardiovascular genetics 20150915 6
<h4>Background</h4>Patients with PCSK9 gene gain of function (GOF) mutations have a rare form of autosomal dominant hypercholesterolemia. However, data examining their clinical characteristics and geographic distribution are lacking. Furthermore, no randomized treatment study in this population has been reported.<h4>Methods and results</h4>We compiled clinical characteristics of PCSK9 GOF mutation carriers in a multinational retrospective, cross-sectional, observational study. We then performed ...[more]