Author Correction: Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation.
Saved in:
| Title: | Author Correction: Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation. |
|---|---|
| Authors: | Ruan, Dan-dan1 (AUTHOR), Ruan, Xing-lin2 (AUTHOR), Wang, Ruo‑li1,3 (AUTHOR), Lin, Xin-fu1,4 (AUTHOR), Zhang, Yan-ping1 (AUTHOR), Lin, Bin1 (AUTHOR), Li, Shi-jie1 (AUTHOR), Wu, Min1 (AUTHOR), Chen, Qian1 (AUTHOR), Zhang, Jian-hui1 (AUTHOR), Cheng, Qiong1,5 (AUTHOR), Zhang, Yi-wu6 (AUTHOR), Lin, Fan1,7 (AUTHOR) linfan@fjmu.edu.cn, Luo, Jie-wei1 (AUTHOR) docluo0421@aliyun.com, Zheng, Zheng1,5 (AUTHOR) zz128cy@163.com, Li, Yun-fei1,5 (AUTHOR) lyfd02068@163.com |
| Source: | Scientific Reports. 9/10/2024, Vol. 14 Issue 1, p1-1. 1p. |
| Database: | Academic Search Ultimate |
|
Full text is not displayed to guests.
Login for full access.
|
|
| FullText | Links: – Type: pdflink Text: Availability: 1 |
|---|---|
| Header | DbId: asn DbLabel: Academic Search Ultimate An: 179554058 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: Author Correction: Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Ruan%2C+Dan-dan%22">Ruan, Dan-dan</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ruan%2C+Xing-lin%22">Ruan, Xing-lin</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wang%2C+Ruo‑li%22">Wang, Ruo‑li</searchLink><relatesTo>1,3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lin%2C+Xin-fu%22">Lin, Xin-fu</searchLink><relatesTo>1,4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhang%2C+Yan-ping%22">Zhang, Yan-ping</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lin%2C+Bin%22">Lin, Bin</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Li%2C+Shi-jie%22">Li, Shi-jie</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wu%2C+Min%22">Wu, Min</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Chen%2C+Qian%22">Chen, Qian</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhang%2C+Jian-hui%22">Zhang, Jian-hui</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Cheng%2C+Qiong%22">Cheng, Qiong</searchLink><relatesTo>1,5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhang%2C+Yi-wu%22">Zhang, Yi-wu</searchLink><relatesTo>6</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lin%2C+Fan%22">Lin, Fan</searchLink><relatesTo>1,7</relatesTo> (AUTHOR)<i> linfan@fjmu.edu.cn</i><br /><searchLink fieldCode="AR" term="%22Luo%2C+Jie-wei%22">Luo, Jie-wei</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> docluo0421@aliyun.com</i><br /><searchLink fieldCode="AR" term="%22Zheng%2C+Zheng%22">Zheng, Zheng</searchLink><relatesTo>1,5</relatesTo> (AUTHOR)<i> zz128cy@163.com</i><br /><searchLink fieldCode="AR" term="%22Li%2C+Yun-fei%22">Li, Yun-fei</searchLink><relatesTo>1,5</relatesTo> (AUTHOR)<i> lyfd02068@163.com</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Scientific+Reports%22">Scientific Reports</searchLink>. 9/10/2024, Vol. 14 Issue 1, p1-1. 1p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=179554058 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1038/s41598-024-72293-3 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 1 StartPage: 1 Titles: – TitleFull: Author Correction: Clinical phenotype and genetic function analysis of a family with hypomyelinating leukodystrophy-7 caused by POLR3A mutation. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Ruan, Dan-dan – PersonEntity: Name: NameFull: Ruan, Xing-lin – PersonEntity: Name: NameFull: Wang, Ruo‑li – PersonEntity: Name: NameFull: Lin, Xin-fu – PersonEntity: Name: NameFull: Zhang, Yan-ping – PersonEntity: Name: NameFull: Lin, Bin – PersonEntity: Name: NameFull: Li, Shi-jie – PersonEntity: Name: NameFull: Wu, Min – PersonEntity: Name: NameFull: Chen, Qian – PersonEntity: Name: NameFull: Zhang, Jian-hui – PersonEntity: Name: NameFull: Cheng, Qiong – PersonEntity: Name: NameFull: Zhang, Yi-wu – PersonEntity: Name: NameFull: Lin, Fan – PersonEntity: Name: NameFull: Luo, Jie-wei – PersonEntity: Name: NameFull: Zheng, Zheng – PersonEntity: Name: NameFull: Li, Yun-fei IsPartOfRelationships: – BibEntity: Dates: – D: 10 M: 09 Text: 9/10/2024 Type: published Y: 2024 Identifiers: – Type: issn-print Value: 20452322 Numbering: – Type: volume Value: 14 – Type: issue Value: 1 Titles: – TitleFull: Scientific Reports Type: main |
| ResultId | 1 |