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Publication date
2016 09 01
Authors
Haack, TB Ignatius, E Calvo-Garrido, J Iuso, A Isohanni, P Maffezzini, C Lonnqvist, T Suomalainen, A Gorza, M Kremer, LS Graf, E Hartig, M Berutti, R Paucar, M Svenningsson, P Stranneheim, H Brandberg, G Wedell, A Kurian, MA Hayflick, SA Venco, P Tiranti, V Strom, TM Dichgans, M Horvath, R Holinski-Feder, E Freyer, C Meitinger, T Prokisch, H Senderek, J Wredenberg, A Carroll, CJ Klopstock, T
Author KI Usernames
Calvo-Garrido, J|javcal Freyer, C|chrfre Maffezzini, C|cammaf Paucar, M|marpau Stranneheim, H|henstr Svenningsson, P|persve Wedell, A|annwed Wredenberg, A|annwre
Pubmed ID
27545679
Journal
American journal of human genetics
Doctype
Article
KI Connection
Medel
Mesh SV
Ataxi Autofagi Autofagosomer Barn Bristfälligt uttal Fenotyp Fibroblaster Gång Kognitiva störningar Kvinnlig Manlig Mitokondrier Människa Neurodegenerativa sjukdomar Onormal muskelspänning RNA, budbärar Rörelserubbningar Stamtavla Supranukleär pares, progressiv Unga vuxna Ungdomar Vuxna Ålder vid sjukdomsdebut
Mesh EN
Age of Onset Ataxia Autophagosomes Autophagy Cognition Disorders Dysarthria Dystonia Fibroblasts Gait Mitochondria Movement Disorders Neurodegenerative Diseases Pedigree Phenotype RNA, Messenger Sequestosome-1 Protein Supranuclear Palsy, Progressive
First date
2016-10-16T10:11:40.612Z