Exome sequencing unravels genetic variants associated with chronic kidney disease in Saudi Arabian patients-Reference-Cited by-同舟云学术

Exome sequencing unravels genetic variants associated with chronic kidney disease in Saudi Arabian patients

Published:2022-10-08 Issue:12 Volume:43 Page:
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Al‐Hamed Mohamed H.¹²^ORCID,Hussein Maged H.³,Shah Yaser⁴,Al‐Mojalli Hamad⁴,Alsabban Essam⁵,Alshareef Turki⁵,Altayyar Ali³,Elshouny Samir³,Ali Wafaa¹,Abduljabbar Mai¹,AlOtaibi Afaf¹,AlShammasi Amal¹,Akili Rana¹,Abouelhoda Mohamed¹,Sayer John A.⁶⁷,Dasouki Majed J.¹,Imtiaz Faiqa¹²

Affiliation:

1. Centre for Genomic Medicine, King Faisal Specialist Hospital and Research Centre Riyadh Saudi Arabia

2. Saudi Diagnostics Laboratory KFSH&RC Riyadh Saudi Arabia

3. Medicine Department, Nephrology Section, KFSH&RC Riyadh Saudi Arabia

4. Organ Transplant Centre of Excellence, Adult Transplant Nephrology KFSH&RC Riyadh Saudi Arabia

5. Pediatric Nephrology KFSH&RC Riyadh Saudi Arabia

6. Translational and Clinical Research Institute, Faculty of Medical Sciences Newcastle University Newcastle upon Tyne UK

7. Renal Services, The Newcastle upon Tyne Hospitals NHS Foundation Trust Newcastle upon Tyne UK

Publisher

Hindawi Limited

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.24480

Reference38 articles.

1. Epidemiology and Outcome of CKD in Omani Children

2. Bialleleic PKD1 mutations underlie early-onset autosomal dominant polycystic kidney disease in Saudi Arabian families

3. Genetic spectrum of Saudi Arabian patients with antenatal cystic kidney disease and ciliopathy phenotypes using a targeted renal gene panel

4. Genetics and genomic medicine in Saudi Arabia

5. Genetic Susceptibility to Chronic Kidney Disease – Some More Pieces for the Heritability Puzzle

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