Genetic spectrum and clinical characteristics of 3β-hydroxy-Δ5-C27-steroid oxidoreductase (HSD3B7) deficiency in China.
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| Title: | Genetic spectrum and clinical characteristics of 3β-hydroxy-Δ5-C |
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| Authors: | Zhao, Jing1 (AUTHOR), Setchell, Kenneth D. R.2 (AUTHOR), Gong, Ying3 (AUTHOR), Sun, Yinghua4 (AUTHOR), Zhang, Ping5 (AUTHOR), Heubi, James E.6 (AUTHOR), Fang, Lingjuan1 (AUTHOR), Lu, Yi1 (AUTHOR), Xie, Xinbao1 (AUTHOR), Gong, Jingyu7 (AUTHOR), Wang, Jian-She1,8 (AUTHOR) jshwang@shmu.edu.cn |
| Source: | Orphanet Journal of Rare Diseases. 10/9/2021, Vol. 16 Issue 1, p1-15. 15p. |
| Database: | Academic Search Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 152927580 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Genetic spectrum and clinical characteristics of 3β-hydroxy-Δ<superscript>5</superscript>-C<subscript>27</subscript>-steroid oxidoreductase (HSD3B7) deficiency in China. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Zhao%2C+Jing%22">Zhao, Jing</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Setchell%2C+Kenneth+D%2E+R%2E%22">Setchell, Kenneth D. R.</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Gong%2C+Ying%22">Gong, Ying</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Sun%2C+Yinghua%22">Sun, Yinghua</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhang%2C+Ping%22">Zhang, Ping</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Heubi%2C+James+E%2E%22">Heubi, James E.</searchLink><relatesTo>6</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Fang%2C+Lingjuan%22">Fang, Lingjuan</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lu%2C+Yi%22">Lu, Yi</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Xie%2C+Xinbao%22">Xie, Xinbao</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Gong%2C+Jingyu%22">Gong, Jingyu</searchLink><relatesTo>7</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wang%2C+Jian-She%22">Wang, Jian-She</searchLink><relatesTo>1,8</relatesTo> (AUTHOR)<i> jshwang@shmu.edu.cn</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 10/9/2021, Vol. 16 Issue 1, p1-15. 15p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=152927580 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13023-021-02041-7 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 15 StartPage: 1 Titles: – TitleFull: Genetic spectrum and clinical characteristics of 3β-hydroxy-Δ5-C27-steroid oxidoreductase (HSD3B7) deficiency in China. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Zhao, Jing – PersonEntity: Name: NameFull: Setchell, Kenneth D. R. – PersonEntity: Name: NameFull: Gong, Ying – PersonEntity: Name: NameFull: Sun, Yinghua – PersonEntity: Name: NameFull: Zhang, Ping – PersonEntity: Name: NameFull: Heubi, James E. – PersonEntity: Name: NameFull: Fang, Lingjuan – PersonEntity: Name: NameFull: Lu, Yi – PersonEntity: Name: NameFull: Xie, Xinbao – PersonEntity: Name: NameFull: Gong, Jingyu – PersonEntity: Name: NameFull: Wang, Jian-She IsPartOfRelationships: – BibEntity: Dates: – D: 09 M: 10 Text: 10/9/2021 Type: published Y: 2021 Identifiers: – Type: issn-print Value: 17501172 Numbering: – Type: volume Value: 16 – Type: issue Value: 1 Titles: – TitleFull: Orphanet Journal of Rare Diseases Type: main |
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