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Interlaboratory development and validation of a HRM method applied to the detection of JAK2 exon 12 mutations in polycythemia vera patients.
Ugo V, Tondeur S, Menot ML, Bonnin N, Le Gac G, Tonetti C, Mansat-De Mas V, Lecucq L, Kiladjian JJ, Chomienne C, Dosquet C, Parquet N, Darnige L, Porneuf M, Escoffre-Barbe M, Giraudier S, Delabesse E, Cassinat B; French Intergroup of Myeloproliferative disorders. Ugo V, et al. Among authors: le gac g. PLoS One. 2010 Jan 26;5(1):e8893. doi: 10.1371/journal.pone.0008893. PLoS One. 2010. PMID: 20126644 Free PMC article.
A new point mutation in EPOR inducing a short deletion in congenital erythrocytosis.
Chauveau A, Luque Paz D, Lecucq L, Le Gac G, Le Maréchal C, Gueguen P, Berthou C, Ugo V. Chauveau A, et al. Among authors: le gac g, le marechal c. Br J Haematol. 2016 Feb;172(3):475-7. doi: 10.1111/bjh.13511. Epub 2015 May 26. Br J Haematol. 2016. PMID: 26010769 Free article. No abstract available.
Nramp2 analysis in hemochromatosis probands.
Le Gac G, Mura C, Raguenes O, Mercier AY, de Braekeleer M, Férec C. Le Gac G, et al. Blood Cells Mol Dis. 2000 Aug;26(4):312-9. doi: 10.1006/bcmd.2000.0312. Blood Cells Mol Dis. 2000. PMID: 11042033
82 results