RT @StefanBarakat: thrilled to see program of #ESHG2020 continuing today! Join our PhD student @EPerenthaler at 11 am in the neurogenetics…
RT @StefanBarakat: thrilled to see program of #ESHG2020 continuing today! Join our PhD student @EPerenthaler at 11 am in the neurogenetics…
thrilled to see program of #ESHG2020 continuing today! Join our PhD student @EPerenthaler at 11 am in the neurogenetics session for our latest results on the UGP2-disease that we described earlier this year, or read https://t.co/OsjLa2OJQl #raredisease #e
RT @StefanBarakat: just a few days to go before our PhD student @EPerenthaler will present at #eshg2020 our latest results on the UGP2-dise…
just a few days to go before our PhD student @EPerenthaler will present at #eshg2020 our latest results on the UGP2-disease that we described earlier this year. Come and join us on Monday at 11 am! or read https://t.co/OsjLa2OJQl #raredisease #epilepsy #U
RT @StefanBarakat: @ejhg_journal #cgscgg2020 I hope the video presentation works well, and otherwise, please have a look at our recent pape…
@ejhg_journal #cgscgg2020 I hope the video presentation works well, and otherwise, please have a look at our recent paper on this work https://t.co/wMwUy2MMLq
@clingensoc looking forward to the #CGSCGG2020 meeting and presenting our recent findings on the new UGP2 epileptic encephalopathy that we have recently published https://t.co/kFCl7DfX4L
in this collaboration https://t.co/cKmO6YCd3i, we find another epileptic encephalopathy gene involved in glucose metabolism, just downstream of the new epilepsy gene UGP2 which my lab recently described in Acta Neuropathologica https://t.co/kFCl7DfX4L
Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases. https://t.co/T0rTeFj7QW
Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases. https://t.co/F3VDnhDk3f
our latest paper: Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential ge... - PubMed - NCBI https://t.co/0Vw93uk3jo
Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases. https://t.co/GJOhIktRQQ #Neuralstemcells
RT @StefanBarakat: Loss of UGP2 in brain causes a severe epileptic encephalopathy: first big paper of the Barakat lab is now online: https…
@neuroliege : and now also available as peer review paper in Acta Neuropathologica: https://t.co/EdUX26aCt7 Spread the news!
Loss of UGP2 in brain causes a severe epileptic encephalopathy: first big paper of the Barakat lab is now online: https://t.co/EdUX26aCt7 many congrats to my team members and the many contributing collaborators!