Exome sequencing in high and low fetal haemoglobin Arab-Indian haplotype sickle cell disease

Journal article

Open access

Peer reviewed

British journal of haematology, Vol.194(2), pp.e61-e64

07/2021

PMID: 34041755

Abstract

Adolescent

Adult

Anemia, Sickle Cell - genetics

Cohort Studies

Exome - genetics

Female

Fetal Hemoglobin - genetics

Haplotypes

Hemoglobins, Abnormal - genetics

Humans

Male

Middle Aged

Polymorphism, Single Nucleotide

Young Adult

url

https://doi.org/10.1111/bjh.17542View

Published (Version of record) Open

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Title: Exome sequencing in high and low fetal haemoglobin Arab-Indian haplotype sickle cell disease
Creators - without role: Awatif N Alnafie - Imam Abdulrahman Bin Faisal University
Suad A Alateeq - Imam Abdulrahman Bin Faisal University
Fahad A Al-Muhanna - King Fahd Hospital of the University
Ahmed M Alsulaiman - King Fahd Hospital, Alhafof, Saudi Arabia
Mohammed Alfarhan - King Faisal University
Waleed Buali - Imam Abdulrahman Bin Faisal University
Chitti Babu Vatte - Imam Abdulrahman Bin Faisal University
Cyril Cyrus - Imam Abdulrahman Bin Faisal University
Brendan Keating - University of Pennsylvania
Amein K Al-Ali - Imam Abdulrahman Bin Faisal University
Martin H Steinberg - Boston University
Publication Details: British journal of haematology, Vol.194(2), pp.e61-e64
Identifiers: 9914541908331
Academic Unit: Imam Abdulrahman Bin Faisal University; King Faisal University
Language: English
Resource Type: Journal article