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Plos One|December 27, 2014
Characterization of the MeCP2R168X knockin mouse model for Rett syndromeEike Wegener, Cornelia Brendel, Andre Fischer, et al.International Journal of Molecular Sciences|July 29, 2023
Evaluation of Novel Enhancer Compounds in Gentamicin-Mediated Readthrough of Nonsense Mutations in Rett SyndromeKeit Men Wong, Eike Wegener, Alireza Baradaran-Heravi, et al.BMC Neurology|May 22, 2016
Compound heterozygous variants in PGAP1 causing severe psychomotor retardation, brain atrophy, recurrent apneas and delayed myelination: a case report and literature reviewMatthias Kettwig, Orly Elpeleg, Eike Wegener, et al.European Journal of Human Genetics : EJHG|August 14, 2014
Tectonic gene mutations in patients with Joubert syndromePeter Huppke, Eike Wegener, Helena Böhrer-Rabel, et al.Journal of Molecular Medicine (Berlin, Germany)|December 2, 2010
Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse modelCornelia Brendel, Valery Belakhov, Hauke Werner, et al.Experimental Neurology|May 28, 2019
Homozygous NMNAT2 mutation in sisters with polyneuropathy and erythromelalgiaPeter Huppke, Eike Wegener, Jonathan Gilley, et al.BMC Medicine|July 6, 2011
MIA is a potential biomarker for tumour load in neurofibromatosis type 1Mateusz Kolanczyk, Victor Mautner, Nadine Kossler, et al.Pageof 1