A novel mutation in USF1 gene is associated with familial combined hyperlipidemia

Author:

Taghizadeh Eskandar12ORCID,Mirzaei Farzaneh1,Jalilian Nazanin3,Ghayour Mobarhan Majid4ORCID,Ferns Gordon A.5,Pasdar Alireza167ORCID

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. Department of Clinical biochemistry, School of MedicineKermanshah University of Medical Sciences Kermanshah Iran

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

5. Department of Medical EducationBrighton and Sussex Medical School Perso Falmer Brighton UK

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

7. Division of Applied Medicine, Medical School, University of Aberdeen Foresterhill Aberdeen UK

Funder

Mashhad University of Medical Sciences

Publisher

Wiley

Subject

Cell Biology,Clinical Biochemistry,Genetics,Molecular Biology,Biochemistry

Reference34 articles.

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

2. Genetics of familial combined hyperlipidemia and risk of coronary heart disease

3. Prevalence and expression of familial combined hyperlipidemia in childhood

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

5. Molecular mechanisms, prevalence, and molecular methods for familial combined hyperlipidemia disease: A review

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