Identification of pathogenic genes associated with CKD: An integrated bioinformatics approach.

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Bibliographic Details
Title: Identification of pathogenic genes associated with CKD: An integrated bioinformatics approach.
Authors: Ahmed MM; Centre for Interdisciplinary Research in Basic Sciences, Jamia Millia Islamia, New Delhi, India., Shafat Z; Centre for Interdisciplinary Research in Basic Sciences, Jamia Millia Islamia, New Delhi, India., Tazyeen S; Centre for Interdisciplinary Research in Basic Sciences, Jamia Millia Islamia, New Delhi, India., Ali R; Centre for Interdisciplinary Research in Basic Sciences, Jamia Millia Islamia, New Delhi, India.; Department of Biosciences, Faculty of Natural Sciences, Jamia Millia Islamia, New Delhi, India., Almashjary MN; Department of Medical Laboratory Sciences, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia., Al-Raddadi R; Community Medicine Department, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Harakeh S; King Fahd Medical Research Center, and Yousef Abdullatif Jameel Chair of Prophetic Medicine Application, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia., Alam A; Centre for Interdisciplinary Research in Basic Sciences, Jamia Millia Islamia, New Delhi, India., Haque S; Research and Scientific Studies Unit, College of Nursing and Allied Health Sciences, Jazan University, Jazan, Saudi Arabia., Ishrat R; Centre for Interdisciplinary Research in Basic Sciences, Jamia Millia Islamia, New Delhi, India.
Source: Frontiers in genetics [Front Genet] 2022 Aug 11; Vol. 13, pp. 891055. Date of Electronic Publication: 2022 Aug 11 (Print Publication: 2022).
Publication Type: Journal Article
Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1664-8021
DOI:10.3389/fgene.2022.891055