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Exome sequencing identifies rare mutations of LDLR and QTRT1 conferring risk for early-onset coronary artery disease in Chinese
| Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9429139/ https://www.ncbi.nlm.nih.gov/pubmed/36060302 http://dx.doi.org/10.1093/nsr/nwac102 |
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| author | Yao, Kang Dai, Yuxiang Shen, Juan Wang, Yi Yang, Huanjie Wu, Runda Liao, Qijun Wu, Hongyi Fang, Xiaodong Shali, Shalaimaiti Xu, Lili Hao, Meng Lin, Chenhao Sun, Zhonghan Liu, Yilian Li, Mengxin Wang, Zhen Gao, Qiang Zhang, Shuning Li, Chenguang Gao, Wei Ge, Lei Zou, Yunzeng Sun, Aijun Qian, Juying Jin, Li Hong, Shangyu Zheng, Yan Ge, Junbo |
| author_facet | Yao, Kang Dai, Yuxiang Shen, Juan Wang, Yi Yang, Huanjie Wu, Runda Liao, Qijun Wu, Hongyi Fang, Xiaodong Shali, Shalaimaiti Xu, Lili Hao, Meng Lin, Chenhao Sun, Zhonghan Liu, Yilian Li, Mengxin Wang, Zhen Gao, Qiang Zhang, Shuning Li, Chenguang Gao, Wei Ge, Lei Zou, Yunzeng Sun, Aijun Qian, Juying Jin, Li Hong, Shangyu Zheng, Yan Ge, Junbo |
| author_sort | Yao, Kang |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-9429139 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2022 |
| publisher | Oxford University Press |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-94291392022-09-01 Exome sequencing identifies rare mutations of LDLR and QTRT1 conferring risk for early-onset coronary artery disease in Chinese Yao, Kang Dai, Yuxiang Shen, Juan Wang, Yi Yang, Huanjie Wu, Runda Liao, Qijun Wu, Hongyi Fang, Xiaodong Shali, Shalaimaiti Xu, Lili Hao, Meng Lin, Chenhao Sun, Zhonghan Liu, Yilian Li, Mengxin Wang, Zhen Gao, Qiang Zhang, Shuning Li, Chenguang Gao, Wei Ge, Lei Zou, Yunzeng Sun, Aijun Qian, Juying Jin, Li Hong, Shangyu Zheng, Yan Ge, Junbo Natl Sci Rev Brief Communication Oxford University Press 2022-05-31 /pmc/articles/PMC9429139/ /pubmed/36060302 http://dx.doi.org/10.1093/nsr/nwac102 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of China Science Publishing & Media Ltd. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
| spellingShingle | Brief Communication Yao, Kang Dai, Yuxiang Shen, Juan Wang, Yi Yang, Huanjie Wu, Runda Liao, Qijun Wu, Hongyi Fang, Xiaodong Shali, Shalaimaiti Xu, Lili Hao, Meng Lin, Chenhao Sun, Zhonghan Liu, Yilian Li, Mengxin Wang, Zhen Gao, Qiang Zhang, Shuning Li, Chenguang Gao, Wei Ge, Lei Zou, Yunzeng Sun, Aijun Qian, Juying Jin, Li Hong, Shangyu Zheng, Yan Ge, Junbo Exome sequencing identifies rare mutations of LDLR and QTRT1 conferring risk for early-onset coronary artery disease in Chinese |
| title | Exome sequencing identifies rare mutations of LDLR and QTRT1 conferring risk for early-onset coronary artery disease in Chinese |
| title_full | Exome sequencing identifies rare mutations of LDLR and QTRT1 conferring risk for early-onset coronary artery disease in Chinese |
| title_fullStr | Exome sequencing identifies rare mutations of LDLR and QTRT1 conferring risk for early-onset coronary artery disease in Chinese |
| title_full_unstemmed | Exome sequencing identifies rare mutations of LDLR and QTRT1 conferring risk for early-onset coronary artery disease in Chinese |
| title_short | Exome sequencing identifies rare mutations of LDLR and QTRT1 conferring risk for early-onset coronary artery disease in Chinese |
| title_sort | exome sequencing identifies rare mutations of ldlr and qtrt1 conferring risk for early-onset coronary artery disease in chinese |
| topic | Brief Communication |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9429139/ https://www.ncbi.nlm.nih.gov/pubmed/36060302 http://dx.doi.org/10.1093/nsr/nwac102 |
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