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Article

MEFV mutations affecting pyrin amino acid 577 cause autosomal dominant autoinflammatory disease

16 Mar 2013

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 23505238
DOI: 10.1136/annrheumdis-2012-202580

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MEFV mutations affecting pyrin amino acid 577 cause autosomal dominant autoinflammatory diseasePMID 23505238Read ↗

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The pyrin family of fever genes: unmasking genetic determinants of autoinflammatory disease.Semantic proximity Read ↗

A dominant pathogenic MEFV mutation causes atypical pyrin-associated periodic syndromes.Semantic proximity Read ↗

New Diseases Linked to MEFV Variants or Pyrinopathies.Semantic proximity Read ↗

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Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle–Wells syndromeSemantic proximity Read ↗

A genotype-first approach reveals the molecular basis of pyrin inflammasome activation.Semantic proximity Read ↗

The expanding spectrum of systemic autoinflammatory disorders and their rheumatic manifestations.Semantic proximity Read ↗

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