Exploring Missense Variants in the Human PNPLA3 Protein: An In Silico Analysis

Background: Missense variants in humans are genetic variations that lead to amino acid substitutions in protein-coding regions, which can modify protein structure, function, and phenotype. The Patatin-like phospholipase domain-containing protein 3 (PNPLA3) gene has received considerable attention b...

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Bibliographic Details
Main Authors: Asia Awad AbdelGader, Afra M. Al Bakry, Hind A. Elnasri, Dawelbiet Abdelaal Yahia, Mona Abdelrahman Mohamed Khaier
Format: Article
Language:English
Published: Knowledge E 2025-06-01
Series:Sudan Journal of Medical Sciences
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Online Access:https://knepublishing.com/index.php/SJMS/article/view/16301
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