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A Familial Case of Childhood Ataxia with Leukodystrophy Due to Novel POLR1C Mutations

Detalles Bibliográficos
Autores principales: Han, Ji Yeon, Kim, Soo Yeon, Cheon, Jung-Eun, Choi, Murim, Lee, Jin Sook, Chae, Jong-Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neurological Association 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7174127/
https://www.ncbi.nlm.nih.gov/pubmed/32319256
http://dx.doi.org/10.3988/jcn.2020.16.2.338
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author Han, Ji Yeon
Kim, Soo Yeon
Cheon, Jung-Eun
Choi, Murim
Lee, Jin Sook
Chae, Jong-Hee
author_facet Han, Ji Yeon
Kim, Soo Yeon
Cheon, Jung-Eun
Choi, Murim
Lee, Jin Sook
Chae, Jong-Hee
author_sort Han, Ji Yeon
collection PubMed
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spelling pubmed-71741272020-04-23 A Familial Case of Childhood Ataxia with Leukodystrophy Due to Novel POLR1C Mutations Han, Ji Yeon Kim, Soo Yeon Cheon, Jung-Eun Choi, Murim Lee, Jin Sook Chae, Jong-Hee J Clin Neurol Letter to the Editor Korean Neurological Association 2020-04 2019-04-02 /pmc/articles/PMC7174127/ /pubmed/32319256 http://dx.doi.org/10.3988/jcn.2020.16.2.338 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
Han, Ji Yeon
Kim, Soo Yeon
Cheon, Jung-Eun
Choi, Murim
Lee, Jin Sook
Chae, Jong-Hee
A Familial Case of Childhood Ataxia with Leukodystrophy Due to Novel POLR1C Mutations
title A Familial Case of Childhood Ataxia with Leukodystrophy Due to Novel POLR1C Mutations
title_full A Familial Case of Childhood Ataxia with Leukodystrophy Due to Novel POLR1C Mutations
title_fullStr A Familial Case of Childhood Ataxia with Leukodystrophy Due to Novel POLR1C Mutations
title_full_unstemmed A Familial Case of Childhood Ataxia with Leukodystrophy Due to Novel POLR1C Mutations
title_short A Familial Case of Childhood Ataxia with Leukodystrophy Due to Novel POLR1C Mutations
title_sort familial case of childhood ataxia with leukodystrophy due to novel polr1c mutations
topic Letter to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7174127/
https://www.ncbi.nlm.nih.gov/pubmed/32319256
http://dx.doi.org/10.3988/jcn.2020.16.2.338
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