Reversible splenial lesion syndrome (RESLES) due to acute intermittent porphyria with a novel mutation in the hydroxymethylbilane synthase gene.
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| Title: | Reversible splenial lesion syndrome (RESLES) due to acute intermittent porphyria with a novel mutation in the hydroxymethylbilane synthase gene. |
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| Authors: | Yang, Jing1 (AUTHOR), Han, Fei2 (AUTHOR), Chen, Qianlong3 (AUTHOR), Zhu, Tienan4 (AUTHOR), Zhao, Yongqiang4 (AUTHOR), Yu, Xuezhong1 (AUTHOR), Zhu, Huadong1 (AUTHOR), Cao, Jian5 (AUTHOR), Li, Xiaoqing6 (AUTHOR) lixiaoqing20060417@126.com |
| Source: | Orphanet Journal of Rare Diseases. 4/19/2020, Vol. 15 Issue 1, p1-5. 5p. |
| Database: | Academic Search Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 142792449 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Reversible splenial lesion syndrome (RESLES) due to acute intermittent porphyria with a novel mutation in the hydroxymethylbilane synthase gene. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Yang%2C+Jing%22">Yang, Jing</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Han%2C+Fei%22">Han, Fei</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Chen%2C+Qianlong%22">Chen, Qianlong</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhu%2C+Tienan%22">Zhu, Tienan</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhao%2C+Yongqiang%22">Zhao, Yongqiang</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Yu%2C+Xuezhong%22">Yu, Xuezhong</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhu%2C+Huadong%22">Zhu, Huadong</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Cao%2C+Jian%22">Cao, Jian</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Li%2C+Xiaoqing%22">Li, Xiaoqing</searchLink><relatesTo>6</relatesTo> (AUTHOR)<i> lixiaoqing20060417@126.com</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 4/19/2020, Vol. 15 Issue 1, p1-5. 5p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=142792449 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13023-020-01375-y Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 5 StartPage: 1 Titles: – TitleFull: Reversible splenial lesion syndrome (RESLES) due to acute intermittent porphyria with a novel mutation in the hydroxymethylbilane synthase gene. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Yang, Jing – PersonEntity: Name: NameFull: Han, Fei – PersonEntity: Name: NameFull: Chen, Qianlong – PersonEntity: Name: NameFull: Zhu, Tienan – PersonEntity: Name: NameFull: Zhao, Yongqiang – PersonEntity: Name: NameFull: Yu, Xuezhong – PersonEntity: Name: NameFull: Zhu, Huadong – PersonEntity: Name: NameFull: Cao, Jian – PersonEntity: Name: NameFull: Li, Xiaoqing IsPartOfRelationships: – BibEntity: Dates: – D: 19 M: 04 Text: 4/19/2020 Type: published Y: 2020 Identifiers: – Type: issn-print Value: 17501172 Numbering: – Type: volume Value: 15 – Type: issue Value: 1 Titles: – TitleFull: Orphanet Journal of Rare Diseases Type: main |
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