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

BMJ Publishing Group, RMD Open, 1(2), p. e000196, 2016

Journal article published in 2016 by Laurent Messer, Hans R. Waterham, Ghada Alsaleh, Philippe Georgel, Raphael Carapito

, Siamak Bahram, Jean Sibilia

This paper is made freely available by the publisher.

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