Whole‐exome sequencing of a Saudi epilepsy cohort reveals association signals in known and potentially novel loci

Journal article

Open access

Peer reviewed

Human genomics, Vol.16(1), pp.71-71

20/12/2022

PMID: 36539902

Abstract

Epilepsy

Neurological conditions

Saudi Arabia

Variants

WES

url

https://doi.org/10.1186/s40246-022-00444-6View

Published (Version of record) Open

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Title: Whole‐exome sequencing of a Saudi epilepsy cohort reveals association signals in known and potentially novel loci
Creators - without role: Abdulrahman H. Al Anazi - King Fahd Hospital of the University
Ahmed S. Ammar - Imam Abdulrahman Bin Faisal University
Mahmoud Al-Hajj - Department of Neurosurgery, King Fahd Hospital, Alhafof, Saudi Arabia
Cyril Cyrus - Imam Abdulrahman Bin Faisal University
Danah Aljaafari - King Fahd Hospital of the University
Iname Khoda - King Fahd Hospital of the University
Ahmed K. Abdelfatah - King Fahd Hospital of the University
Abdullah A. Alsulaiman - Imam Abdulrahman Bin Faisal University
Firas Alanazi - Imam Abdulrahman Bin Faisal University
Rawan Alanazi - King Fahd Hospital of the University
Divya Gandla - University of Pennsylvania
Hetal Lad - University of Pennsylvania
Samar Barayan - Imam Abdulrahman Bin Faisal University
Brendan J. Keating - University of Pennsylvania
Amein K. Al-Ali - Imam Abdulrahman Bin Faisal University
Publication Details: Human genomics, Vol.16(1), pp.71-71
Publisher: BioMed Central
Grant note: 14-MED81-46 / ;
Identifiers: 9914793108331
Academic Unit: Imam Abdulrahman Bin Faisal University
Language: English
Resource Type: Journal article