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Double trouble? Progranulin mutation and C9ORF72 repeat expansion in a case of primary non-fluent aphasia.
- Source :
-
Journal of the neurological sciences [J Neurol Sci] 2014 Jun 15; Vol. 341 (1-2), pp. 176-8. Date of Electronic Publication: 2014 Mar 19. - Publication Year :
- 2014
- Subjects :
- Cerebral Cortex diagnostic imaging
Cerebral Cortex pathology
Female
Fluorodeoxyglucose F18
Humans
Magnetic Resonance Imaging
Middle Aged
Middle Cerebral Artery physiopathology
Positron-Emission Tomography
Primary Progressive Nonfluent Aphasia diagnosis
Progranulins
Radiography
Spin Labels
Intercellular Signaling Peptides and Proteins genetics
Mutation genetics
Primary Progressive Nonfluent Aphasia genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1878-5883
- Volume :
- 341
- Issue :
- 1-2
- Database :
- MEDLINE
- Journal :
- Journal of the neurological sciences
- Publication Type :
- Report
- Accession number :
- 24703252
- Full Text :
- https://doi.org/10.1016/j.jns.2014.03.030