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Clinical heterogeneity within the ALS-FTD spectrum in a family with a homozygous optineurin mutation

Document Type

Article

Author

Parvizi, T.; Keritam, O.; Caliskan, H.; Imhof, S.; König, T.; Zimprich, A.; Rath, J.; Stögmann, E.; Cetin, H.; Klotz, S.; Gelpi, E.; Haider, L.; Traub-Weidinger, T.; Wagner, M.; Brunet, T.; Brugger, M.

Source

In: Annals of Clinical and Translational Neurology. (Annals of Clinical and Translational Neurology, 2024)

Subject

Language

English

ISSN

23289503

Online Access

Full Text (Gale Academic Onefile) Full Text (ProQuest Central) Open Access (Wiley) Web of Science JCR 저널정보 Scopus Find it@PNU

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