Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleA homozygous GDAP2 loss-of-function variant in a patient with adult-onset cerebellar ataxia.AuthorsBreza, Marianthi; Bourinaris, Thomas; Efthymiou, Stephanie; Maroofian, Reza; Athanasiou-Fragkouli, Alkyoni; Tzartos, John; Velonakis, Georgios; Karavasilis, Efstratios; Angelopoulou, Georgia; Kasselimis, Dimitrios; Potagas, Constantin; Stefanis, Leonidas; Karadima, Georgia; Koutsis, Georgios; Houlden, HenrySubjectsCEREBELLAR ataxia; SPINOCEREBELLAR ataxia; SOCIOBIOLOGY; NEUROMUSCULAR diseases; FRIEDREICH'S ataxia; RESEARCH institutes; GENETIC mutation; PATIENTS; GENOTYPESPublicationBrain: A Journal of Neurology, 2020, Vol 143, Issue 6, pe49ISSN0006-8950Publication typeletterDOI10.1093/brain/awaa120