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J Neurol Sci. 2014 Jun 15;341(1-2):176-8. doi: 10.1016/j.jns.2014.03.030. Epub 2014 Mar 19.

Double trouble? Progranulin mutation and C9ORF72 repeat expansion in a case of primary non-fluent aphasia.

Author information

1
Department of Medicine, Surgery and Neurosciences, University of Siena, Italy.
2
Unit of Functional Rehabilitation, Azienda Ospedaliera di Siena, Italy.
3
Unit of Diagnostic and Therapeutic Neuroradiology, Azienda Ospedaliera di Siena, Italy.
4
Unit of Nuclear Medicine, Azienda Ospedaliera di Siena, Italy.
5
Consiglio Sanitario Regionale, Regione Toscana, Italy.
6
Department of Laboratory Medicine, Azienda Ospedaliera Città della Salute e della Scienza di Torino, Italy.
7
Department of Medicine, Surgery and Neurosciences, University of Siena, Italy. Electronic address: dotti@unisi.it.

KEYWORDS:

C9ORF72; Frontotemporal lobar degeneration (FTLD); Primary non-fluent aphasia (PNFA); Progranulin (GRN)

PMID:
24703252
DOI:
10.1016/j.jns.2014.03.030
[Indexed for MEDLINE]

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