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Epilepsy & Behavior : E&B|March 12, 2014
CHD2 mutations in Lennox-Gastaut syndromeCaroline Lund, Eylert Brodtkorb, Ane-Marte Øye, et al.European Journal of Medical Genetics|October 18, 2015
Generalized epilepsy in a family with basal ganglia calcifications and mutations in SLC20A2 and CHRNB2Roar Fjaer, Eylert Brodtkorb, Ane-Marte Øye, et al.Molecular Genetics and Metabolism|July 5, 2017
Biochemical and genetic characterization of an unusual mild PEX3-related Zellweger spectrum disorderKathrine Bjørgo, Roar Fjær, Hanne Håberg Mørk, et al.Human Molecular Genetics|December 24, 2016
Novel UCHL1 mutations reveal new insights into ubiquitin processingSiri L Rydning, Paul H Backe, Mirta M L Sousa, et al.Human Molecular Genetics|June 14, 2021
A novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge-Weber syndromeRoar Fjær, Katarzyna Marciniak, Olav Sundnes, et al.Pageof 1