Frontotemporal dementia with a C9ORF72 expansion in a Swedish family: clinical and neuropathological characteristics.
Research output: Contribution to journal › Article
In 2011 the C9ORF72 repeat expansion was identified as the most frequent genetic mutation underlying FTD and ALS. The main aim of this study was to investigate clinical characteristics in a large C9ORF72-positive FTD family, and to compare these with the neuropathological findings.
|Research areas and keywords||
Subject classification (UKÄ) – MANDATORY
|Journal||American Journal of Neurodegenerative Disease|
|Publication status||Published - 2013|
The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Pathology, (Lund) (013030000), Department of Psychogeriatrics (013304000)
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Related research output
Maria Landqvist, 2014, Department of Psychogeriatrics, Department of Clinical Sciences. 120 p.
Research output: Thesis › Doctoral Thesis (compilation)