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Heterozygous TREM2 Mutation in Semantic Variant of Primary Progressive Aphasia

Detalles Bibliográficos
Autores principales: Ji, Min-Jin, Jung, Sungwon, Seo, Ha-Eun, Kim, Sang-Young, Kim, Woo-Ram, Kim, Sora, Lee, Jin Sook, Noh, Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neurological Association 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7174111/
https://www.ncbi.nlm.nih.gov/pubmed/32319261
http://dx.doi.org/10.3988/jcn.2020.16.2.352
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author Ji, Min-Jin
Jung, Sungwon
Seo, Ha-Eun
Kim, Sang-Young
Kim, Woo-Ram
Kim, Sora
Lee, Jin Sook
Noh, Young
author_facet Ji, Min-Jin
Jung, Sungwon
Seo, Ha-Eun
Kim, Sang-Young
Kim, Woo-Ram
Kim, Sora
Lee, Jin Sook
Noh, Young
author_sort Ji, Min-Jin
collection PubMed
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spelling pubmed-71741112020-04-23 Heterozygous TREM2 Mutation in Semantic Variant of Primary Progressive Aphasia Ji, Min-Jin Jung, Sungwon Seo, Ha-Eun Kim, Sang-Young Kim, Woo-Ram Kim, Sora Lee, Jin Sook Noh, Young J Clin Neurol Letter to the Editor Korean Neurological Association 2020-04 2020-04-02 /pmc/articles/PMC7174111/ /pubmed/32319261 http://dx.doi.org/10.3988/jcn.2020.16.2.352 Text en Copyright © 2020 Korean Neurological Association http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letter to the Editor
Ji, Min-Jin
Jung, Sungwon
Seo, Ha-Eun
Kim, Sang-Young
Kim, Woo-Ram
Kim, Sora
Lee, Jin Sook
Noh, Young
Heterozygous TREM2 Mutation in Semantic Variant of Primary Progressive Aphasia
title Heterozygous TREM2 Mutation in Semantic Variant of Primary Progressive Aphasia
title_full Heterozygous TREM2 Mutation in Semantic Variant of Primary Progressive Aphasia
title_fullStr Heterozygous TREM2 Mutation in Semantic Variant of Primary Progressive Aphasia
title_full_unstemmed Heterozygous TREM2 Mutation in Semantic Variant of Primary Progressive Aphasia
title_short Heterozygous TREM2 Mutation in Semantic Variant of Primary Progressive Aphasia
title_sort heterozygous trem2 mutation in semantic variant of primary progressive aphasia
topic Letter to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7174111/
https://www.ncbi.nlm.nih.gov/pubmed/32319261
http://dx.doi.org/10.3988/jcn.2020.16.2.352
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