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  • Lesca Gaetan, Ville Dorothée, Milh Mathieu, Villard Laurent, Afenjar Alexandra, Mignot Cyril, Nava Caroline, Gérard Marion, Perrin Laurence, Doummar Diane, Auvin Stéphane, Hempel Maja, Knoers Nine, Biskup Saskia, Hörtnagel Konstanze, Bast Thomas, Striano Pasquale, Fontana Elena, Zara Federico, Linnet Karen M., Moog Ute, Lederer Damien, Van Coster Rudy, Lagae Lieven, Hjalgrim Helle, Helbig Katherine L., Hardies Katia, De Jonghe Peter, Weckhuysen Sarah, Krägeloh-Mann Ingeborg, Helbig Ingo, Kluger Gerhard. Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders. Brain - A Journal of Neurology , Oxford University Press (OUP), 2017, 140 (5), pp.1316-1336. ⟨10.1093/brain/awx054⟩
  • Lesca Gaetan, Ville Dorothée, Milh Mathieu, Villard Laurent, Afenjar Alexandra, Chantot-Bastaraud Sandra, Mignot Cyril, Nava Caroline, Gérard Marion, Perrin Laurence, Doummar Diane, Auvin Stéphane, Hempel Maja, Knoers Nine, Biskup Saskia, Hörtnagel Konstanze, Bast Thomas, Striano Pasquale, Fontana Elena, Zara Federico, Linnet Karen M., Moog Ute, Lederer Damien, van Coster Rudy, Lagae Lieven, Hjalgrim Helle, Helbig Katherine L., Hardies Katia, de Jonghe Peter, Weckhuysen Sarah, Krägeloh-Mann Ingeborg, Helbig Ingo, Kluger Gerhard. Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders. Brain - A Journal of Neurology , 2017, 140 (5), pp.1316-1336. ⟨10.1093/brain/awx054⟩
Title
  • Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders
dc:date
  • 2017
Digital Object Identifier (DOI)
  • 10.1093/brain/awx054
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