A Novel Phosphoinositide-3-kinase Adapter Protein 1 Gene Missense Mutation in Familial Cirrhosis

Familial cirrhosis is a condition that is associated with the presence of liver disease with genetic linkage among multiple family members in a generation or in multiple generations. With cirrhosis, most of these disease pathogeneses are related to a defect of an enzyme/transport protein leading to...

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Bibliografske podrobnosti
izdano v:J Clin Exp Hepatol
Main Authors: Abby Philips, Cyriac, Agarwal, Meenal, Phadke, Nikhil, Rajesh, Sasidharan, Padsalgi, Guruprasad, Ahamed, Rizwan, Augustine, Philip
Format: Artigo
Jezik:Inglês
Izdano: Elsevier 2019
Teme:
Case Report
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6823681/
https://ncbi.nlm.nih.gov/pubmed/31695254
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jceh.2019.02.002
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