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1 Ergebnisse
1
Genetic Prion Disease Caused by PRNP Q160X Mutation Present..:
Fong, Jamie C
;
Rojas, Julio C
;
Bang, Jee
...
qt36d0g2kt. , 2017
Link:
https://escholarship.org/uc/item/36d0g2kt
RT Journal T1
Genetic Prion Disease Caused by PRNP Q160X Mutation Presenting with an Orbitofrontal Syndrome, Cyclic Diarrhea, and Peripheral Neuropathy
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt36d0g2kt&Exemplar=1&LAN=DE A1 Fong, Jamie C A1 Rojas, Julio C A1 Bang, Jee A1 Legati, Andrea A1 Rankin, Katherine P A1 Forner, Sven A1 Miller, Zachary A A1 Karydas, Anna M A1 Coppola, Giovanni A1 Grouse, Carrie K A1 Ralph, Jeffrey A1 Miller, Bruce L A1 Geschwind, Michael D PB eScholarship, University of California YR 2017 K1 Biomedical and Clinical Sciences K1 Neurosciences K1 Clinical Sciences K1 Brain Disorders K1 Acquired Cognitive Impairment K1 Rare Diseases K1 Clinical Research K1 Peripheral Neuropathy K1 Dementia K1 Neurodegenerative K1 Genetics K1 2.1 Biological and endogenous factors K1 Aetiology K1 Neurological K1 Adult K1 Brain K1 Codon K1 Nonsense K1 Disease Progression K1 Follow-Up Studies K1 Humans K1 Longitudinal Studies K1 Male K1 Pedigree K1 Peripheral Nerves K1 Phenotype K1 Prion Diseases K1 Prion Proteins K1 Amyloidosis K1 DNA sequencing K1 dysautonomia K1 exome K1 mutation K1 prion dementia K1 Cognitive Sciences K1 Neurology & Neurosurgery K1 Biological psychology JF qt36d0g2kt LK http://dx.doi.org/https://escholarship.org/uc/item/36d0g2kt DO https://escholarship.org/uc/item/36d0g2kt SF ELIB - SuUB Bremen
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