Molecular insights into the coding region mutations of low‐density lipoprotein receptor adaptor protein 1 (LDLRAP1) linked to familial hypercholesterolemia-Reference-Cited by-同舟云学术

Molecular insights into the coding region mutations of low‐density lipoprotein receptor adaptor protein 1 (LDLRAP1) linked to familial hypercholesterolemia

Published:2020-03-03 Issue:6 Volume:22 Page:
ISSN:1099-498X
Container-title:The Journal of Gene Medicine
language:en
Short-container-title:J Gene Med

Author:

Shaik Noor A.¹²,Al‐Qahtani Faten¹,Nasser Khalidah²³,Jamil Kaiser⁴,Alrayes Nuha Mohammad²³,Elango Ramu¹²,Awan Zuhier Ahmed⁵,Banaganapalli Babajan¹²^ORCID

Affiliation:

1. Department of Genetic Medicine, Faculty of MedicineKing Abdulaziz University Jeddah Saudi Arabia

2. Princess Al‐Jawhara Al‐Brahim Center of Excellence in Research of Hereditary DisordersKing Abdulaziz University Jeddah Saudi Arabia

3. Department of Medical Laboratory Technology, Faculty of Applied Medical SciencesKing Abdulaziz University Jeddah Saudi Arabia

4. Deptartment of GeneticsBhagwan Mahavir Medical Research Centre Hyderabad India

5. Department of Clinical Biochemistry, Faculty of MedicineKing Abdulaziz University Jeddah Saudi Arabia

Funder

King Abdulaziz University

Publisher

Wiley

Subject

Genetics (clinical),Drug Discovery,Genetics,Molecular Biology,Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jgm.3176

Reference34 articles.

1. Hyperlipidemia as a Risk Factor for Cardiovascular Disease

2. Polygenic Hypercholesterolemia and Cardiovascular Disease Risk

3. The history of Autosomal Recessive Hypercholesterolemia (ARH). From clinical observations to gene identification

4. Novel combined variants of LDLR and LDLRAP1 genes causing severe familial hypercholesterolemia

5. The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine

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