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Article

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

22 Oct 2001

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 11687797
DOI: 10.1038/ng756

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Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle–Wells syndromePMID 11687797Read ↗

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MEFV mutations affecting pyrin amino acid 577 cause autosomal dominant autoinflammatory diseaseSemantic proximity Read ↗

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