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Reply to: No evidence supports genetic heterogeneity of neuronal intranuclear inclusion disease

Detalles Bibliográficos
Autores principales: Chen, Zhongbo, Ryten, Mina, Houlden, Henry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732245/
https://www.ncbi.nlm.nih.gov/pubmed/33124767
http://dx.doi.org/10.1002/acn3.51222
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author Chen, Zhongbo
Ryten, Mina
Houlden, Henry
author_facet Chen, Zhongbo
Ryten, Mina
Houlden, Henry
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spelling pubmed-77322452020-12-16 Reply to: No evidence supports genetic heterogeneity of neuronal intranuclear inclusion disease Chen, Zhongbo Ryten, Mina Houlden, Henry Ann Clin Transl Neurol Reply To Letter John Wiley and Sons Inc. 2020-10-30 /pmc/articles/PMC7732245/ /pubmed/33124767 http://dx.doi.org/10.1002/acn3.51222 Text en © 2020 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 http://creativecommons.org/licenses/by-nc-nd/4.0/ 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.
spellingShingle Reply To Letter
Chen, Zhongbo
Ryten, Mina
Houlden, Henry
Reply to: No evidence supports genetic heterogeneity of neuronal intranuclear inclusion disease
title Reply to: No evidence supports genetic heterogeneity of neuronal intranuclear inclusion disease
title_full Reply to: No evidence supports genetic heterogeneity of neuronal intranuclear inclusion disease
title_fullStr Reply to: No evidence supports genetic heterogeneity of neuronal intranuclear inclusion disease
title_full_unstemmed Reply to: No evidence supports genetic heterogeneity of neuronal intranuclear inclusion disease
title_short Reply to: No evidence supports genetic heterogeneity of neuronal intranuclear inclusion disease
title_sort reply to: no evidence supports genetic heterogeneity of neuronal intranuclear inclusion disease
topic Reply To Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732245/
https://www.ncbi.nlm.nih.gov/pubmed/33124767
http://dx.doi.org/10.1002/acn3.51222
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