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Phenotype–Genotype Analysis of Cryopyrin-Associated Periodic Syndromes (CAPS): Description of a Rare Non-Exon 3 and a Novel CIAS1 Missense Mutation

Mendelian DisorderPhenotype–genotype AnalysisGenetic DisorderGeneticsMolecular BiologyMolecular GeneticsCryopyrin-associated Periodic SyndromesMedicineRare Non-exon 3