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Page 1
Prevalence and spectrum of mutations in a cohort of 192 unrelated patients with hypertrophic cardiomyopathy.
Millat G, Bouvagnet P, Chevalier P, Dauphin C, Jouk PS, Da Costa A, Prieur F, Bresson JL, Faivre L, Eicher JC, Chassaing N, Crehalet H, Porcher R, Rodriguez-Lafrasse C, Rousson R. Millat G, et al. Among authors: bouvagnet p. Eur J Med Genet. 2010 Sep-Oct;53(5):261-7. doi: 10.1016/j.ejmg.2010.07.007. Epub 2010 Jul 30. Eur J Med Genet. 2010. PMID: 20624503
Spectrum of pathogenic mutations and associated polymorphisms in a cohort of 44 unrelated patients with long QT syndrome.
Millat G, Chevalier P, Restier-Miron L, Da Costa A, Bouvagnet P, Kugener B, Fayol L, Gonzàlez Armengod C, Oddou B, Chanavat V, Froidefond E, Perraudin R, Rousson R, Rodriguez-Lafrasse C. Millat G, et al. Among authors: bouvagnet p. Clin Genet. 2006 Sep;70(3):214-27. doi: 10.1111/j.1399-0004.2006.00671.x. Clin Genet. 2006. PMID: 16922724
TRPM4 non-selective cation channel variants in long QT syndrome.
Hof T, Liu H, Sallé L, Schott JJ, Ducreux C, Millat G, Chevalier P, Probst V, Guinamard R, Bouvagnet P. Hof T, et al. Among authors: bouvagnet p. BMC Med Genet. 2017 Mar 18;18(1):31. doi: 10.1186/s12881-017-0397-4. BMC Med Genet. 2017. PMID: 28315637 Free PMC article.
[Long QT syndrome in children: analysis of the Lyon series].
Iraqi M, Chevalier P, Raboisson MJ, Bozio A, Bouvagnet P, Millat G, Rodriguez-Lafrasse C. Iraqi M, et al. Among authors: bouvagnet p. Arch Mal Coeur Vaiss. 2006 Feb;99(2):134-40. Arch Mal Coeur Vaiss. 2006. PMID: 16555697 French.
A human MYBPC3 mutation appearing about 10 centuries ago results in a hypertrophic cardiomyopathy with delayed onset, moderate evolution but with a risk of sudden death.
Teirlinck CH, Senni F, Malti RE, Majoor-Krakauer D, Fellmann F, Millat G, André-Fouët X, Pernot F, Stumpf M, Boutarin J, Bouvagnet P. Teirlinck CH, et al. Among authors: bouvagnet p. BMC Med Genet. 2012 Nov 10;13:105. doi: 10.1186/1471-2350-13-105. BMC Med Genet. 2012. PMID: 23140321 Free PMC article.
97 results