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A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia

[Image: see text]

Detalles Bibliográficos
Autores principales: Wei, Qiao, Wang, Pei‐Shan, Dong, Hai‐Lin, Luo, Wen‐Jiao, Wu, Zhi‐Ying, Li, Hong‐Fu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034676/
https://www.ncbi.nlm.nih.gov/pubmed/35347897
http://dx.doi.org/10.1002/mgg3.1927
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author Wei, Qiao
Wang, Pei‐Shan
Dong, Hai‐Lin
Luo, Wen‐Jiao
Wu, Zhi‐Ying
Li, Hong‐Fu
author_facet Wei, Qiao
Wang, Pei‐Shan
Dong, Hai‐Lin
Luo, Wen‐Jiao
Wu, Zhi‐Ying
Li, Hong‐Fu
author_sort Wei, Qiao
collection PubMed
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spelling pubmed-90346762022-04-25 A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia Wei, Qiao Wang, Pei‐Shan Dong, Hai‐Lin Luo, Wen‐Jiao Wu, Zhi‐Ying Li, Hong‐Fu Mol Genet Genomic Med Letter to the Editor [Image: see text] John Wiley and Sons Inc. 2022-03-29 /pmc/articles/PMC9034676/ /pubmed/35347897 http://dx.doi.org/10.1002/mgg3.1927 Text en © 2022 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letter to the Editor
Wei, Qiao
Wang, Pei‐Shan
Dong, Hai‐Lin
Luo, Wen‐Jiao
Wu, Zhi‐Ying
Li, Hong‐Fu
A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia
title A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia
title_full A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia
title_fullStr A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia
title_full_unstemmed A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia
title_short A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia
title_sort novel ubap1 truncated variant in a chinese family with hereditary spastic paraplegia
topic Letter to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034676/
https://www.ncbi.nlm.nih.gov/pubmed/35347897
http://dx.doi.org/10.1002/mgg3.1927
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