MVK mutations and associated clinical features in Italian patients affected with autoinflammatory disorders and recurrent fever-Reference-Cited by-同舟云学术

MVK mutations and associated clinical features in Italian patients affected with autoinflammatory disorders and recurrent fever

Published:2004-11-10 Issue:3 Volume:13 Page:314-320
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

D'Osualdo Andrea,Picco Paolo,Caroli Francesco,Gattorno Marco,Giacchino Raffaella,Fortini Patrizia,Corona Fabrizia,Tommasini Alberto,Salvi Giuseppe,Specchia Fernando,Obici Laura,Meini Antonella,Ricci Antonio,Seri Marco,Ravazzolo Roberto,Martini Alberto,Ceccherini Isabella

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/5201323.pdf

Reference23 articles.

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3. van der Meer JW, Vossen JM, Radl J et al: Hyperimmunoglobulinaemia D and periodic fever: a new syndrome. Lancet 1984; 1: 1087–1090.

4. Klasen IS, Goertz JH, van der Wiel GA, Weemaes CM, van der Meer JW, Drenth JP : Hyper-immunoglobulin A in the hyperimmunoglobulinemia D syndrome. Clin Diagn Lab Immunol 2001; 8: 58–61.

5. Drenth JP, Cuisset L, Grateau G et al: Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. Nat Genet 1999; 22: 178–181.

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