Autor/in Milh, Mathieu Afenjar, Alexandra 1 Endele, Sabine 1 Fritsch, Angela 1 Gardella, Elena 1 Geider, Kirsten 1 Hedrich, Ulrike B S 1 Hellenbroich, Yorck 1 Johannesen, Katrine M 1 Kortüm, Fanny 1 Lesca, Gaetan 1 Masnada, Silvia 1 Pientka, Friederike K 1 Popp, Bernt 1 Rosenberger, Georg 1 Rubboli, Guido 1 Stefanova, Irina 1 Tamer, Ceyhun 1 Villard, Laurent 1 Ville, Dorothée 1 Wolff, Markus 1 alle zeigenListe einklappen
Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders Wolff, Markus Johannesen, Katrine M Hedrich, Ulrike B S Masnada, Silvia Rubboli, Guido Gardella, Elena Lesca, Gaetan 2017 - Forschungsinformationssystem des UKE
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes. Endele, Sabine Rosenberger, Georg Geider, Kirsten Popp, Bernt Tamer, Ceyhun Stefanova, Irina Milh, Mathieu 2010 - Forschungsinformationssystem des UKE