Utilizing Whole-Exome Sequencing to Characterize the Phenotypic Variability of Sickle Cell Disease-Reference-Cited by-同舟云学术

Utilizing Whole-Exome Sequencing to Characterize the Phenotypic Variability of Sickle Cell Disease

Published:2018-09 Issue:9 Volume:22 Page:561-567
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Alsultan Abdulrahman¹,Al-Suliman Ahmed M.²,Aleem Aamer³,AlGahtani Farjah H.³,Alfadhel Majid⁴⁵

Affiliation:

1. Department of Pediatrics, College of Medicine, King Saud University, Riyadh, Saudi Arabia.

2. Department of Medicine, King Fahad Hospital, Hofuf, Saudi Arabia.

3. Department of Internal Medicine, College of Medicine, King Saud University, Riyadh, Saudi Arabia.

4. Department of Pediatrics, King Abdullah Specialist Children's Hospital, King Abdullah International Medical Research Centre, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh, Saudi Arabia.

5. King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.

Publisher

Mary Ann Liebert Inc

Subject

Genetics(clinical),General Medicine

Link

https://www.liebertpub.com/doi/pdf/10.1089/gtmb.2018.0058

Reference45 articles.

1. Fetal hemoglobin in sickle cell anemia

2. Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign

3. Sickle Cell Disease Subphenotypes in Patients From Southwestern Province of Saudi Arabia

4. Demands and challenges for patients with sickle-cell disease requiring hematopoietic stem cell transplantation in Saudi Arabia

5. Exome Analysis of Rare and Common Variants within the NOD Signaling Pathway

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