Cascade genetic screening for familial hypercholesterolemia

Cascade genetic screening for familial hypercholesterolemia

Familial hypercholesterolemia (FH) is one of the most common congenital metabolic disorders. Cascade genetic screening used for diagnostic of patients with FH. Aim of study is to explore the awareness of FH patients of the problem of familial hypercholesterolemia and conduct a pilot study of patient...

Full description

Bibliographic Details
Main Authors: M. I. Voevoda, E. V. Shakhtshneider, K. V. Makarenkova, D. E. Ivanoshchuk, P. S. Orlov, Yu. I. Ragino
Format: Article
Language:Russian
Published: Siberian Branch of Russian Academy of Sciences, Research Institute of Internal and Preventive Medicine, branch of the Institute of Cytology and Genetics 2015-12-01
Series:Атеросклероз
Subjects:
cascade genetic screening
familial hypercholesterolemia
low density lipoprotein receptor gene
proprotein convertase subtilisin / kexin 9 gene
apolipoprotein b gene
mutations
Online Access:https://ateroskleroz.elpub.ru/jour/article/view/774/712

Internet

https://ateroskleroz.elpub.ru/jour/article/view/774/712

Similar Items