A novel variant in LPL gene is associated with familial combined hyperlipidemia-Reference-Cited by-同舟云学术

A novel variant in LPL gene is associated with familial combined hyperlipidemia

Author:

Taghizadeh Eskandar¹²^ORCID,Ghayour‐Mobarhan Majid³^ORCID,Ferns Gordon A.⁴,Pasdar Alireza¹⁵⁶^ORCID

Affiliation:

1. Department of Medical Genetics, Faculty of MedicineMashhad University of Medical Sciences Mashhad Iran

2. Cellular and Molecular Research CenterYasuj University of Medical Sciences Yasuj Iran

3. Metabolic Syndrome Research Centre, School of MedicineMashhad University of Medical Sciences Mashhad Iran

4. Department of Medical EducationBrighton and Sussex Medical School Brighton UK

5. Medical Genetics Research Centre, Faculty of MedicineMashhad University of Medical Sciences Mashhad Iran

6. Division of Applied Medicine, Medical SchoolUniversity of Aberdeen Aberdeen UK

Funder

Mashhad University of Medical Sciences

Publisher

Wiley

Subject

Clinical Biochemistry,Molecular Medicine,General Medicine,Biochemistry

Link

Reference37 articles.

1. Familial combined hyperlipidemia: Current knowledge, perspectives, and controversies;Bello‐Chavolla OY;Rev Invest Clin,2018

3. Practical guidelines for familial combined hyperlipidemia diagnosis: An up‐date;Gaddi A;Vasc Health Risk Manag,2007

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