Letter to the editor on: Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions by Park et al. (2022)
Huihui Luo(Queen Mary University of London), Zhongbo Chen(Institute of Human Genetics), Dennis W. Dickson(Jacksonville College), Tamás Révész(UCL Australia), Gábor G. Kovács(University Health Network), John Hardy(UK Dementia Research Institute), Michael DeTure(Jacksonville College), Dominic B. Rowe(Macquarie University), Emily P. McCann(Centre National de la Recherche Scientifique), Stéphanie Efthymiou(Queen Mary University of London), Natalia Dominik(National Hospital for Neurology and Neurosurgery), Mina Ryten(Guy's Hospital), Kylie Montgomery(New England Biolabs (United States)), Glenda M. Halliday(The University of Sydney), Ellen Gelpí(Consorci Institut D'Investigacions Biomediques August Pi I Sunyer), Laura Molina‐Porcel(Institute of Human Genetics), Tammaryn Lashley(National Hospital for Neurology and Neurosurgery), Ian P. Blair(Macquarie University), Anu Suomalainen(University of Helsinki), Kristina Zhelcheska(National Hospital for Neurology and Neurosurgery), Zane Jaunmuktane(King's College London), Andrew J. Lees(Centre for Movement Disorders), Hannah Macpherson(University College London), Emil K. Gustavsson(University of British Columbia), Pentti J. Tienari(University of Helsinki), Henry Houlden(Queen Mary University of London), Arianna Tucci(Genomics England), Wai Yan Yau(Perron Institute for Neurological and Translational Science), Matti Haltia(University of Helsinki), Chris Turner(National Hospital for Neurology and Neurosurgery), Claire Anderson(Great Ormond Street Hospital), Keith A. Josephs(Mayo Clinic)
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