Clinical heterogeneity within the ALS-FTD spectrum in a family with a homozygous optineurin mutation.
Parvizi T, Klotz S, Keritam O, Caliskan H, Imhof S, König T, Haider L, Traub-Weidinger T, Wagner M, Brunet T, Brugger M, Zimprich A, Rath J, Stögmann E, Gelpi E, Cetin H.
Parvizi T, et al. Among authors: caliskan h.
Ann Clin Transl Neurol. 2024 Apr 30. doi: 10.1002/acn3.52075. Online ahead of print.
Ann Clin Transl Neurol. 2024.
PMID: 38689506
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