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.
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.
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  Data: Prolidase deficiency, a rare inborn error of immunity, clinical phenotypes, immunological features, and proposed treatments in twins.
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  Data: <searchLink fieldCode="JN" term="%22Allergy%2C+Asthma+%26+Clinical+Immunology%22">Allergy, Asthma & Clinical Immunology</searchLink>. 2/23/2022, Vol. 18 Issue 1, p1-11. 11p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=155396622
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        Value: 10.1186/s13223-022-00658-2
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        Text: English
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      – TitleFull: Prolidase deficiency, a rare inborn error of immunity, clinical phenotypes, immunological features, and proposed treatments in twins.
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            NameFull: Alrumayyan, Nora
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            NameFull: Slauenwhite, Drew
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            NameFull: Issekutz, Thomas B.
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              Text: 2/23/2022
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              Y: 2022
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