Screening of LDLR and APOB gene mutations in Mexican patients with homozygous familial hypercholesterolemia-Reference-Cited by-同舟云学术

Screening of LDLR and APOB gene mutations in Mexican patients with homozygous familial hypercholesterolemia

Published:2018-05 Issue:3 Volume:12 Page:693-701
ISSN:1933-2874
Container-title:Journal of Clinical Lipidology
language:en
Short-container-title:Journal of Clinical Lipidology

Author:

Hernández Flores Teresita De Jesús,González García Juan Ramón,Colima Fausto Ana Gabriela,Vázquez Cárdenas Norma Alejandra,Sánchez López Yoaly,Zarate Morales César Augusto,Magaña Torres María Teresa

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Nutrition and Dietetics,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference60 articles.

1. Familial Hypercholesterolemia;Brown;Metab Mol Bases Inherit Dis,2007

2. Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: consensus statement of the European Atherosclerosis Society;Nordestgaard;Eur Heart J,2013

3. Systems glycobiology: Integrating glycogenomics, glycoproteomics, glycomics, and other 'Omics Data Sets to characterize cellular glycosylation processes;Bennun;J Mol Biol,2016

4. Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society;Cuchel;Eur Heart J,2014

5. New approaches in detection and treatment of familial hypercholesterolemia;Hartgers;Curr Cardiol Rep,2015

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1. High Prevalence of Familial Hypercholesterolemia Due to the Founder Effect of the LDLR c.2271del Variant in Communities of Oaxaca, Mexico;Archives of Medical Research;2024-04

2. A novel loop-mediated isothermal amplification-based genotyping method and its application for identifying proprotein convertase subtilisin/kexin type 9 variants in familial hypercholesterolemia;Biochimica et Biophysica Acta (BBA) - General Subjects;2022-02

3. The LDLR c.501C>A is a disease-causing variant in familial hypercholesterolemia;Lipids in Health and Disease;2021-09-12

4. LDLR Gene Mutation p.Asp360His and Familial Hypercholesterolemia in a Mexican Community;Archives of Medical Research;2020-02