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Article

Somatic NLRP3 mosaicism in Muckle-Wells syndrome. A genetic mechanism shared by different phenotypes of cryopyrin-associated periodic syndromes

11 Dec 2013

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 24326009
DOI: 10.1136/annrheumdis-2013-204361

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Somatic NLRP3 mosaicism in Muckle-Wells syndrome. A genetic mechanism shared by different phenotypes of cryopyrin-associated periodic syndromesPMID 24326009Read ↗

The role of somatic NLRP3 mosaicism and new gene discovery in mutation negative cryopyrin-associated periodic syndrome patientsSemantic proximity Read ↗

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Brief Report: Cryopyrin-Associated Periodic Syndrome Caused by a Myeloid-Restricted Somatic NLRP3 Mutation.Semantic proximity Read ↗

Muckle-Wells syndrome: a rare hereditary cryopyrin-associated periodic syndrome.Semantic proximity Read ↗

Novel Insights into the Clinical Features, Genetic Spectrum and Clonal Evolution of Patients Carrying NLRP3 Mosaicism.Semantic proximity Read ↗

Clinical Features, Outcomes of Treatments, Inflammasome Function and Longitudinal Clonal Dynamics into<i>NLRP3</i>Mosaicism: Evidence from the Largest Cryopyrin-associated Periodic Syndromes Cohort to DateSemantic proximity Read ↗

An Adult Patient With a Novel Mutation in NLRP3 Gene Associated With Cryopyrin-Associated Periodic Syndrome Mimicking Adult-Onset Still Disease.Semantic proximity Read ↗

First report of vertical transmission of a somatic NLRP3 mutation in cryopyrin-associated periodic syndromes.Semantic proximity Read ↗

Three generations of suffering: cryopyrin-associated periodic syndrome with NLRP3 mutation in a family.Semantic proximity Read ↗

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