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Reply: Genetic heterogeneity of neuronal intranuclear inclusion disease. What about the infantile variant?

Yau, WY; Chen, Z; Sullivan, R; Vandrovcova, J; Houlden, H; (2021) Reply: Genetic heterogeneity of neuronal intranuclear inclusion disease. What about the infantile variant? Annals of Clinical and Translational Neurology , 8 (4) pp. 1002-1004. 10.1002/acn3.51330. Green open access

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Type: Article
Title: Reply: Genetic heterogeneity of neuronal intranuclear inclusion disease. What about the infantile variant?
Location: United States
Open access status: An open access version is available from UCL Discovery
DOI: 10.1002/acn3.51330
Publisher version: https://doi.org/10.1002/acn3.51330
Language: English
Additional information: © 2021 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Department of Neuromuscular Diseases
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Neurodegenerative Diseases
URI: https://discovery.ucl.ac.uk/id/eprint/10125795
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