Molecular mechanisms, prevalence, and molecular methods for familial combined hyperlipidemia disease: A review-Reference-Cited by-同舟云学术

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

Author:

Taghizadeh Eskandar¹²,Mardani Rajab³,Rostami Daryoush⁴,Taghizadeh Hassan²,Bazireh Homa⁵,Hayat Seyed Mohammad Gheibi⁶^ORCID

Affiliation:

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

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

3. Department of Biochemistry Pasteur Institute of Iran Tehran Iran

4. Department of School Allied Zabol University of Medical Sciences Zabol Iran

5. Department of Industrial and Environmental Biotechnology National Institute of Genetic Engineering and Biotechnology Tehran Iran

6. Department of Medical Genetics School of Medicine, Shahid Sadoughi University of Medical Science Yazd Iran

Publisher

Wiley

Subject

Cell Biology,Molecular Biology,Biochemistry

Link

Reference47 articles.

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

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