Prolidase deficiency, a rare inborn error of immunity, clinical phenotypes, immunological features, and proposed treatments in twins.
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| Title: | Prolidase deficiency, a rare inborn error of immunity, clinical phenotypes, immunological features, and proposed treatments in twins. |
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| Authors: | Alrumayyan, Nora1 (AUTHOR), Slauenwhite, Drew1 (AUTHOR), McAlpine, Sarah M.1 (AUTHOR), Roberts, Sarah1 (AUTHOR), Issekutz, Thomas B.1 (AUTHOR), Huber, Adam M.2 (AUTHOR), Liu, Zaiping3 (AUTHOR), Derfalvi, Beata1 (AUTHOR) beata.derfalvi@iwk.nshealth.ca |
| Source: | Allergy, Asthma & Clinical Immunology. 2/23/2022, Vol. 18 Issue 1, p1-11. 11p. |
| 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: 155396622 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13223-022-00658-2 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 11 StartPage: 1 Titles: – TitleFull: Prolidase deficiency, a rare inborn error of immunity, clinical phenotypes, immunological features, and proposed treatments in twins. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Alrumayyan, Nora – PersonEntity: Name: NameFull: Slauenwhite, Drew – PersonEntity: Name: NameFull: McAlpine, Sarah M. – PersonEntity: Name: NameFull: Roberts, Sarah – PersonEntity: Name: NameFull: Issekutz, Thomas B. – PersonEntity: Name: NameFull: Huber, Adam M. – PersonEntity: Name: NameFull: Liu, Zaiping – PersonEntity: Name: NameFull: Derfalvi, Beata IsPartOfRelationships: – BibEntity: Dates: – D: 23 M: 02 Text: 2/23/2022 Type: published Y: 2022 Identifiers: – Type: issn-print Value: 17101484 Numbering: – Type: volume Value: 18 – Type: issue Value: 1 Titles: – TitleFull: Allergy, Asthma & Clinical Immunology Type: main |
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