Development of therapies for rare genetic disorders of GPX4: roadmap and opportunities.
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| Title: | Development of therapies for rare genetic disorders of GPX4: roadmap and opportunities. |
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| Authors: | Cheff, Dorian M.1,2 (AUTHOR), Muotri, Alysson R.3,4 (AUTHOR), Stockwell, Brent R.5,6 (AUTHOR), Schmidt, Edward E.7 (AUTHOR), Ran, Qitao8,9 (AUTHOR), Kartha, Reena V.10 (AUTHOR), Johnson, Simon C.11,12,13 (AUTHOR), Mittal, Plavi14 (AUTHOR), Arnér, Elias S. J.2,15 (AUTHOR), Wigby, Kristen M.16,17 (AUTHOR), Hall, Matthew D.1 (AUTHOR), Ramesh, Sanath Kumar18 (AUTHOR) sanath@GPX4.org |
| Source: | Orphanet Journal of Rare Diseases. 10/23/2021, Vol. 16 Issue 1, p1-15. 15p. |
| 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: 153184412 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=153184412 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13023-021-02048-0 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 15 StartPage: 1 Titles: – TitleFull: Development of therapies for rare genetic disorders of GPX4: roadmap and opportunities. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Cheff, Dorian M. – PersonEntity: Name: NameFull: Muotri, Alysson R. – PersonEntity: Name: NameFull: Stockwell, Brent R. – PersonEntity: Name: NameFull: Schmidt, Edward E. – PersonEntity: Name: NameFull: Ran, Qitao – PersonEntity: Name: NameFull: Kartha, Reena V. – PersonEntity: Name: NameFull: Johnson, Simon C. – PersonEntity: Name: NameFull: Mittal, Plavi – PersonEntity: Name: NameFull: Arnér, Elias S. J. – PersonEntity: Name: NameFull: Wigby, Kristen M. – PersonEntity: Name: NameFull: Hall, Matthew D. – PersonEntity: Name: NameFull: Ramesh, Sanath Kumar IsPartOfRelationships: – BibEntity: Dates: – D: 23 M: 10 Text: 10/23/2021 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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