Progressive aphasia as the presenting symptom in a patient with amyotrophic lateral sclerosis with a novel mutation in the OPTN gene

David CzellNeuromuscular Diseases Unit/ALS Clinic, Kantonsspital St.Gallen, St.Gallen, SwitzerlandCorrespondence[email protected]

Peter M. AndersenInstitute of Pharmacology and Clinical Neuroscience, Umeå University, Umeå, Sweden

Christoph NeuwirthNeuromuscular Diseases Unit/ALS Clinic, Kantonsspital St.Gallen, St.Gallen, Switzerland

Mitsuya MoritaDepartment of Neurology, Jichi Medical University, Yakushiji, Shimotsuke-shi, Japan

Markus WeberNeuromuscular Diseases Unit/ALS Clinic, Kantonsspital St.Gallen, St.Gallen, Switzerland;Department of Neurology, University Hospital Basel, Basel, Switzerland

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Declaration of interest: The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.

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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

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