Journal Article (Letter)

DZNE-2020-04221

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png Paranoid delusion as lead symptom in two siblings with late-onset Tay-Sachs disease and a novel mutation in the HEXA gene.

Stendel, C. (First author)DZNE* ; Gallenmüller, C.DZNE* ; Peters, K. ; Bürger, F. ; Gramer, G. ; Biskup, S. ; Klopstock, T. (Last author)DZNE*

2015
Springer73057 Berlin

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Please use a persistent id in citations: doi:10.1007/s00415-015-7729-0

Keyword(s): Adult (MeSH) ; Age of Onset (MeSH) ; Delusions: etiology (MeSH) ; Delusions: physiopathology (MeSH) ; Female (MeSH) ; Humans (MeSH) ; Male (MeSH) ; Mutation (MeSH) ; Paranoid Disorders: etiology (MeSH) ; Paranoid Disorders: physiopathology (MeSH) ; Siblings (MeSH) ; Tay-Sachs Disease: complications (MeSH) ; Tay-Sachs Disease: genetics (MeSH) ; Tay-Sachs Disease: physiopathology (MeSH) ; Young Adult (MeSH) ; beta-Hexosaminidase alpha Chain: genetics (MeSH) ; HEXA protein, human ; beta-Hexosaminidase alpha Chain

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Contributing Institute(s):

1. Translational Neurodegeneration (AG Höglinger 1)
2. Ext LMU Klinik (Ext LMU Klinik)
3. Clinical Dementia Research München (Clinical Dementia Research München)

Research Program(s):

1. 344 - Clinical and Health Care Research (POF3-344) (POF3-344)

Appears in the scientific report 2015

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Database coverage:
; BIOSIS Previews ; Current Contents - Life Sciences ; Ebsco Academic Search ; IF < 5 ; JCR ; NCBI Molecular Biology Database ; SCOPUS ; Science Citation Index ; Science Citation Index Expanded ; Thomson Reuters Master Journal List ; Web of Science Core Collection

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