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1 Ergebnisse
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Truncating Mutations in UBAP1 Cause Hereditary Spastic Para..:
Farazi Fard M. A
;
Rebelo A. P
;
Buglo E
...
info:eu-repo/semantics/altIdentifier/pmid/30929741. , 2019
Link:
http://hdl.handle.net/2318/1800431
RT Journal T1
Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia
UL https://suche.suub.uni-bremen.de/peid=base-ftunivtorino:oai:iris.unito.it:2318_1800431&Exemplar=1&LAN=DE A1 Farazi Fard M. A A1 Rebelo A. P A1 Buglo E A1 Nemati H A1 Dastsooz H A1 Gehweiler I A1 Reich S A1 Reichbauer J A1 Quintans B A1 Ordonez-Ugalde A A1 Cortese A A1 Courel S A1 Abreu L A1 Powell E A1 Danzi M A1 Martuscelli N. B A1 Bis-Brewer D. M A1 Tao F A1 Zarei F A1 Habibzadeh P A1 Yavarian M A1 Modarresi F A1 Silawi M A1 Tabatabaei Z A1 Yousefi M A1 Farpour H. R A1 Kessler C A1 Mangold E A1 Kobeleva X A1 Mueller A. J A1 Haack T. B A1 Tarnopolsky M A1 Gan-Or Z A1 Rouleau G. A A1 Synofzik M A1 Sobrido M. -J A1 Jordanova A A1 Schule R A1 Zuchner S A1 Faghihi M. A YR 2019 K1 animal model K1 endosomal trafficking K1 genetic disease K1 hereditary spastic paraplegia K1 neurodegenerative disease K1 spasticity K1 ubiquitination K1 zebrafish K1 Adolescent K1 Adult K1 Aged K1 80 and over K1 Animal K1 Carrier Protein K1 Child K1 Preschool K1 Databases K1 Factual K1 Disease Models K1 Endosome K1 Family Health K1 Female K1 Fibroblast K1 Genes K1 Dominant K1 Genetic Linkage K1 Genetic Predisposition to Disease K1 Genomic K1 HEK293 Cell K1 Haploinsufficiency K1 Human K1 Male K1 Middle Aged K1 Pedigree K1 Protein Isoform K1 Spastic Paraplegia K1 Hereditary K1 Young Adult K1 Mutation JF info:eu-repo/semantics/altIdentifier/pmid/30929741 LK http://hdl.handle.net/2318/1800431 DO http://hdl.handle.net/2318/1800431 SF ELIB - SuUB Bremen
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