Comment on: Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype
Author:
Affiliation:
1. Section of Molecular Pathology and Human Genetics, Department of Internal Medicine, School of Medicine, University of Crete , Heraklion, Greece
2. Department of Internal Medicine, University Hospital of Heraklion , Heraklion, Greece
Publisher
Oxford University Press (OUP)
Subject
Pharmacology (medical),Rheumatology
Link
https://academic.oup.com/rheumatology/advance-article-pdf/doi/10.1093/rheumatology/kead102/49512023/kead102.pdf
Reference5 articles.
1. Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype;Özkılınç Önen;Rheumatology (Oxford),2023
2. Familial Mediterranean fever at the millennium. Clinical spectrum, ancient mutations, and a survey of 100 American referrals to the National Institutes of Health;Samuels;Medicine (Baltimore),1998
3. Familial Mediterranean Fever in Crete: a genetic and structural biological approach in a population of intermediate risk;Fragouli;Clin Genet,2008
4. The role of the pro-apoptotic protein Siva in the pathogenesis of Familial Mediterranean fever: a structural and functional analysis;Goulielmos;Biochem Biophys Res Commun,2010
5. Altered expression levels of miR-4520A associated with Familial Mediterranean Fever (FMF);Latsoudis;J Cellular Physiol,2017
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