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bibliographicCitation Swift IJ, Bocchetta M, Benotmane H, Woollacott IO, Shafei R, Rohrer JD. Variable clinical phenotype in TBK1 mutations: case report of a novel mutation causing primary progressive aphasia and review of the literature. Neurobiology of Aging. 2021 Mar;99():100.e9–100.e15. doi: 10.1016/j.neurobiolaging.2020.08.014.
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date 202103
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title Variable clinical phenotype in TBK1 mutations: case report of a novel mutation causing primary progressive aphasia and review of the literature
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