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Multi-OMICS analyses unveil STAT1 as a potential modifier gene in mevalonate kinase deficiency

Crossref DOI link: https://doi.org/10.1136/annrheumdis-2018-213524

Published Print: 2018-11

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Carapito, Raphael

Carapito, Christine

Morlon, Aurore

Paul, Nicodème

Vaca Jacome, Alvaro Sebastian

Alsaleh, Ghada

Rolli, Véronique

Tahar, Ouria

Aouadi, Ismail

Rompais, Magali

Delalande, François

Pichot, Angélique

Georgel, Philippe

Messer, Laurent

Sibilia, Jean

Cianferani, Sarah

Van Dorsselaer, Alain

Bahram, Seiamak
Funding

Funding for this research was provided by:

Institut Universitaire de France

Agence Nationale de la Recherche

MSD AVENIR

Institut National de la Santé et de la Recherche Médicale

European Regional Development Fund

French Proteomic Infrastructure
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Text and Data Mining valid from 2018-11-01

Text and Data Mining valid from 2018-11-01

Version of Record valid from 2018-07-20
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This article is maintained by: Elsevier

Article Title: Multi-OMICS analyses unveil STAT1 as a potential modifier gene in mevalonate kinase deficiency

Journal Title: Annals of the Rheumatic Diseases

CrossRef DOI link to publisher maintained version: https://doi.org/10.1136/annrheumdis-2018-213524

Content Type: article

Copyright: Copyright © 2018 © Author(s) (or their employer(s)) 2018. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by Elsevier Inc. Published by Elsevier B.V. All rights are reserved, including those for text and data mining, AI training, and similar technologies.