Cargando…

A Case of AOA2 With Compound Heterozygous SETX Mutations

Detalles Bibliográficos
Autores principales: Chang, Hee Jin, Kim, Ryul, Kim, Minchae, Moon, Jangsup, Kim, Man Jin, Kim, Han-Joon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Movement Disorder Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9171306/
https://www.ncbi.nlm.nih.gov/pubmed/34937158
http://dx.doi.org/10.14802/jmd.21139
_version_ 1784721635959373824
author Chang, Hee Jin
Kim, Ryul
Kim, Minchae
Moon, Jangsup
Kim, Man Jin
Kim, Han-Joon
author_facet Chang, Hee Jin
Kim, Ryul
Kim, Minchae
Moon, Jangsup
Kim, Man Jin
Kim, Han-Joon
author_sort Chang, Hee Jin
collection PubMed
description
format Online
Article
Text
id pubmed-9171306
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher The Korean Movement Disorder Society
record_format MEDLINE/PubMed
spelling pubmed-91713062022-06-17 A Case of AOA2 With Compound Heterozygous SETX Mutations Chang, Hee Jin Kim, Ryul Kim, Minchae Moon, Jangsup Kim, Man Jin Kim, Han-Joon J Mov Disord Letter to the Editor The Korean Movement Disorder Society 2022-05 2021-12-24 /pmc/articles/PMC9171306/ /pubmed/34937158 http://dx.doi.org/10.14802/jmd.21139 Text en Copyright © 2022 The Korean Movement Disorder Society https://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/ (https://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
Chang, Hee Jin
Kim, Ryul
Kim, Minchae
Moon, Jangsup
Kim, Man Jin
Kim, Han-Joon
A Case of AOA2 With Compound Heterozygous SETX Mutations
title A Case of AOA2 With Compound Heterozygous SETX Mutations
title_full A Case of AOA2 With Compound Heterozygous SETX Mutations
title_fullStr A Case of AOA2 With Compound Heterozygous SETX Mutations
title_full_unstemmed A Case of AOA2 With Compound Heterozygous SETX Mutations
title_short A Case of AOA2 With Compound Heterozygous SETX Mutations
title_sort case of aoa2 with compound heterozygous setx mutations
topic Letter to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9171306/
https://www.ncbi.nlm.nih.gov/pubmed/34937158
http://dx.doi.org/10.14802/jmd.21139
work_keys_str_mv AT changheejin acaseofaoa2withcompoundheterozygoussetxmutations
AT kimryul acaseofaoa2withcompoundheterozygoussetxmutations
AT kimminchae acaseofaoa2withcompoundheterozygoussetxmutations
AT moonjangsup acaseofaoa2withcompoundheterozygoussetxmutations
AT kimmanjin acaseofaoa2withcompoundheterozygoussetxmutations
AT kimhanjoon acaseofaoa2withcompoundheterozygoussetxmutations
AT changheejin caseofaoa2withcompoundheterozygoussetxmutations
AT kimryul caseofaoa2withcompoundheterozygoussetxmutations
AT kimminchae caseofaoa2withcompoundheterozygoussetxmutations
AT moonjangsup caseofaoa2withcompoundheterozygoussetxmutations
AT kimmanjin caseofaoa2withcompoundheterozygoussetxmutations
AT kimhanjoon caseofaoa2withcompoundheterozygoussetxmutations