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Contribution of rare homozygous and compound heterozygous V..:
Stefanie Smolders
;
Stéphanie Philtjens
;
David Crosiers
...
https://doi.org/10.1186/s40478-021-01121-w. , 2021
Link:
https://doi.org/10.1186/s40478-021-01121-w
RT Journal T1
Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease
UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:0fced290715347dcbcc51313cf18c4b6&Exemplar=1&LAN=DE A1 Stefanie Smolders A1 Stéphanie Philtjens A1 David Crosiers A1 Anne Sieben A1 Elisabeth Hens A1 Bavo Heeman A1 Sara Van Mossevelde A1 Philippe Pals A1 Bob Asselbergh A1 Roberto Dos Santos Dias A1 Yannick Vermeiren A1 Rik Vandenberghe A1 Sebastiaan Engelborghs A1 Peter Paul De Deyn A1 Jean-Jacques Martin A1 Patrick Cras A1 Wim Annaert A1 Christine Van Broeckhoven A1 BELNEU consortium PB BMC YR 2021 K1 Lewy body disease K1 Dementia with lewy bodies K1 DLB K1 Parkinson's disease K1 PD K1 Vacuolar protein sorting 13 homolog C K1 Neurology. Diseases of the nervous system K1 RC346-429 JF https://doi.org/10.1186/s40478-021-01121-w LK http://dx.doi.org/https://doi.org/10.1186/s40478-021-01121-w DO https://doi.org/10.1186/s40478-021-01121-w SF ELIB - SuUB Bremen
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