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9. Molecular analysis of the MVK and TNFRSF1A genes in patients with a clinical presentation typical of the hyperimmunoglobulinemia D with periodic fever syndrome: a low-penetrance TNFRSF1A variant in a heterozygous MVK carrier possibly influences the phenotype of hyperimmunoglobulinemia D with periodic fever syndrome or vice versa. Stojanov S; Lohse P; Lohse P; Hoffmann F; Renner ED; Zellerer S; Kéry A; Shin YS; Haas D; Hoffmann GF; Belohradsky BH Arthritis Rheum; 2004 Jun; 50(6):1951-8. PubMed ID: 15188372 [TBL] [Abstract][Full Text] [Related]
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14. A new mutation causing autosomal dominant periodic fever syndrome in a Danish family. Weyhreter H; Schwartz M; Kristensen TD; Valerius NH; Paerregaard A J Pediatr; 2003 Feb; 142(2):191-3. PubMed ID: 12584543 [TBL] [Abstract][Full Text] [Related]
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