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Homozygosity for the V377I mutation in mevalonate kinase causes distinct clinical phenotypes in two sibs with hyperimmunoglobulinaemia D and periodic fever syndrome (HIDS)

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Description scientific article published on 7 March 2016
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author: Raphaël Carapito  Seiamak Bahram  Nassim Dali-youcef  Philippe Georgel 

Publication date March 7, 2016
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