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Progressive aphasia as the presenting symptom in a patient with amyotrophic lateral sclerosis with a novel mutation in the OPTN gene.
Czell D
Neuromuscular Diseases Unit/ALS Clinic, Kantonsspital St.Gallen, St.Gallen, Switzerland. david.czell@gmx.ch
Andersen PM
Neuwirth C
Morita M
Weber M
2013-01-04
Published in:
Amyotrophic lateral sclerosis & frontotemporal degeneration. - 2013
Amyotrophic Lateral Sclerosis
Aphasia
Humans
Male
Middle Aged
Mutation
Transcription Factor TFIIIA
Language
English
Open access status
closed
Identifiers
DOI
10.3109/21678421.2012.756525
PMID
23282279
Persistent URL
https://sonar.ch/global/documents/528
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