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Messer L, Alsaleh G, Georgel P, et al. Homozygosity for the V377I mutation in mevalonate kinase causes distinct clinical phenotypes in two sibs with hyperimmunoglobulinaemia D and periodic fever syndrome (HIDS). RMD Open. 2016;2(1):e000196doi: 10.1136/rmdopen-2015-000196.
Messer, L., Alsaleh, G., Georgel, P., Carapito, R., Waterham, H. R., Dali-Youcef, N., Bahram, S., & Sibilia, J. (2016). Homozygosity for the V377I mutation in mevalonate kinase causes distinct clinical phenotypes in two sibs with hyperimmunoglobulinaemia D and periodic fever syndrome (HIDS). RMD open, 2(1), e000196. https://doi.org/10.1136/rmdopen-2015-000196
Messer, Laurent, et al. "Homozygosity for the V377I mutation in mevalonate kinase causes distinct clinical phenotypes in two sibs with hyperimmunoglobulinaemia D and periodic fever syndrome (HIDS)." RMD open vol. 2,1 (2016): e000196. doi: https://doi.org/10.1136/rmdopen-2015-000196
Messer L, Alsaleh G, Georgel P, Carapito R, Waterham HR, Dali-Youcef N, Bahram S, Sibilia J. Homozygosity for the V377I mutation in mevalonate kinase causes distinct clinical phenotypes in two sibs with hyperimmunoglobulinaemia D and periodic fever syndrome (HIDS). RMD Open. 2016 Mar 07;2(1):e000196. doi: 10.1136/rmdopen-2015-000196. eCollection 2016. PMID: 26977311; PMCID: PMC4785531.
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