Exome Sequencing Identifies the Extremely Rare ITGAV and FN1 Variants in Early Onset Inflammatory Bowel Disease Patients

Journal article

Open access

Peer reviewed

Frontiers in pediatrics, Vol.10, pp.895074-895074

26/05/2022

PMID: 35692981

Abstract

consanguineous

digenic inheritance

early onset-inflammatory bowel disease

gene expression

monogenic diseases

Pediatrics

WES

url

https://doi.org/10.3389/fped.2022.895074View

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Title: Exome Sequencing Identifies the Extremely Rare ITGAV and FN1 Variants in Early Onset Inflammatory Bowel Disease Patients
Creators - without role: Huda Husain Al-Numan - King Abdulaziz University
Rana Mohammed Jan - King Abdulaziz University
Najla bint Saud Al-Saud - , , , , , , , , , , , , , , , , , , , ,
Omran M. Rashidi - Saudi Commission for Health Specialties
Nuha Mohammad Alrayes - King Abdulaziz University
Hadeel A. Alsufyani - King Abdulaziz University
Abdulrahman Mujalli - King Abdulaziz University
Noor Ahmad Shaik - King Abdulaziz University
Mahmoud Hisham Mosli - King Abdulaziz University
Ramu Elango - , , , , , , , , , , , , , , , , , , , ,
Omar I. Saadah - King Abdulaziz University
Babajan Banaganapalli - King Abdulaziz University
Publication Details: Frontiers in pediatrics, Vol.10, pp.895074-895074
Publisher: Frontiers Media S.A
Grant note: ;
Identifiers: 9931690508331
Academic Unit: Umm Al Qura University; King Abdulaziz University
Language: English
Resource Type: Journal article