Cargando…
A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia
[Image: see text]
Autores principales: | , , , , , |
---|---|
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 |
_version_ | 1784693161396797440 |
---|---|
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 |
description | [Image: see text] |
format | Online Article Text |
id | pubmed-9034676 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT weiqiao anovelubap1truncatedvariantinachinesefamilywithhereditaryspasticparaplegia AT wangpeishan anovelubap1truncatedvariantinachinesefamilywithhereditaryspasticparaplegia AT donghailin anovelubap1truncatedvariantinachinesefamilywithhereditaryspasticparaplegia AT luowenjiao anovelubap1truncatedvariantinachinesefamilywithhereditaryspasticparaplegia AT wuzhiying anovelubap1truncatedvariantinachinesefamilywithhereditaryspasticparaplegia AT lihongfu anovelubap1truncatedvariantinachinesefamilywithhereditaryspasticparaplegia AT weiqiao novelubap1truncatedvariantinachinesefamilywithhereditaryspasticparaplegia AT wangpeishan novelubap1truncatedvariantinachinesefamilywithhereditaryspasticparaplegia AT donghailin novelubap1truncatedvariantinachinesefamilywithhereditaryspasticparaplegia AT luowenjiao novelubap1truncatedvariantinachinesefamilywithhereditaryspasticparaplegia AT wuzhiying novelubap1truncatedvariantinachinesefamilywithhereditaryspasticparaplegia AT lihongfu novelubap1truncatedvariantinachinesefamilywithhereditaryspasticparaplegia |