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Open Access 01-11-2013 | Meeting abstract

P02-024 - Clinical impact of V198M mutation in NLRP3 gene

Authors: R Caorsi, A Insalaco, L Obici, L Cantarini, A Meini, M Alessio, L Lepore, F Zulian, F Caroli, I Ceccherini, A Martini, M Gattorno

Excerpt

The V198M mutation is described as a possible hypomorphic variant of the NLPR3 gene. However the impact of this mutation is still largely unknown. …

Title: P02-024 - Clinical impact of V198M mutation in NLRP3 gene
Authors: R Caorsi
A Insalaco
L Obici
L Cantarini
A Meini
M Alessio
L Lepore
F Zulian
F Caroli
I Ceccherini
A Martini
M Gattorno
Publication date: 01-11-2013
Publisher: BioMed Central
Published in: Pediatric Rheumatology / Issue Special Issue 1/2013
Electronic ISSN: 1546-0096
DOI: https://doi.org/10.1186/1546-0096-11-S1-A131