I agree that this site is using cookies. You can find further informations
here
.
X
Login
Merkliste (
0
)
Home
About us
Home About us
Our history
Profile
Press & public relations
Friends
The library in figures
Exhibitions
Projects
Training, internships, careers
Films
Services & Information
Home Services & Information
Lending and interlibrary loans
Returns and renewals
Training and library tours
My Account
Library cards
New to the library?
Download Information
Opening hours
Learning spaces
PC, WLAN, copy, scan and print
Catalogs and collections
Home Catalogs and Collections
Rare books and manuscripts
Digital collections
Subject Areas
Our sites
Home Our sites
Central Library
Law Library (Juridicum)
BB Business and Economics (BB11)
BB Physics and Electrical Engineering
TB Engineering and Social Sciences
TB Economics and Nautical Sciences
TB Music
TB Art & Design
TB Bremerhaven
Contact the library
Home Contact the library
Staff Directory
Open access & publishing
Home Open access & publishing
Reference management: Citavi & RefWorks
Publishing documents
Open Access in Bremen
zur Desktop-Version
Toggle navigation
Merkliste
1 Ergebnisse
1
A novel PRRT2 pathogenic variant in a family with paroxysma..:
Lu, Jacqueline G
;
Bishop, Juliet
;
Cheyette, Sarah
...
qt4pn3p7f9. , 2018
Link:
https://escholarship.org/uc/item/4pn3p7f9
RT Journal T1
A novel PRRT2 pathogenic variant in a family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt4pn3p7f9&Exemplar=1&LAN=DE A1 Lu, Jacqueline G A1 Bishop, Juliet A1 Cheyette, Sarah A1 Zhulin, Igor B A1 Guo, Su A1 Sobreira, Nara A1 Brenner, Steven E PB eScholarship, University of California YR 2018 K1 Biological Sciences K1 Biomedical and Clinical Sciences K1 Genetics K1 Clinical Research K1 Pediatric K1 Neurodegenerative K1 Neurosciences K1 Human Genome K1 2.1 Biological and endogenous factors K1 Aetiology K1 Amino Acid Sequence K1 Base Sequence K1 Child K1 Chromosome Segregation K1 Conserved Sequence K1 Dystonia K1 Epilepsy K1 Benign Neonatal K1 Evolution K1 Molecular K1 Family K1 Female K1 Humans K1 Infant K1 Inheritance Patterns K1 Male K1 Membrane Proteins K1 Mutation K1 Nerve Tissue Proteins K1 Pedigree K1 ataxia K1 autism K1 extrapyramidal dyskinesia K1 focal autonomic seizures without altered responsiveness K1 infantile spasms K1 intellectual disability K1 profound K1 migraine without aura K1 paroxysmal dyskinesia K1 Pharmacology and pharmaceutical sciences JF qt4pn3p7f9 LK http://dx.doi.org/https://escholarship.org/uc/item/4pn3p7f9 DO https://escholarship.org/uc/item/4pn3p7f9 SF ELIB - SuUB Bremen
Export
RefWorks (nur Desktop-Version!)
Flow
(Zuerst in
Flow
einloggen, dann importieren)