Novel PGM3 mutation in two siblings with combined immunodeficiency and childhood bullous pemphigoid: a case report and review of the literature
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1710-1492
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
-
online resource.
- Erschienen in
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Novel PGM3 mutation in two siblings with combined immunodeficiency and childhood bullous pemphigoid: a case report and review of the literature ; volume:18 ; number:1 ; day:24 ; month:12 ; year:2022 ; pages:1-9 ; date:12.2022
Allergy, asthma and clinical immunology ; 18, Heft 1 (24.12.2022), 1-9, 12.2022
- Urheber
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Fallahi, Mazdak
Jamee, Mahnaz
Enayat, Javad
Abdollahimajd, Fahimeh
Mesdaghi, Mehrnaz
Khoddami, Maliheh
Segarra-Roca, Anna
Frohne, Alexandra
Dmytrus, Jasmin
Keramatipour, Mohammad
Mansouri, Mahboubeh
Eslamian, Golnaz
Fallah, Shahrzad
Boztug, Kaan
Chavoshzadeh, Zahra
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s13223-022-00749-0
- URN
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urn:nbn:de:101:1-2023030621124106858452
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
- 14.08.2025, 11:02 MESZ
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Beteiligte
- Fallahi, Mazdak
- Jamee, Mahnaz
- Enayat, Javad
- Abdollahimajd, Fahimeh
- Mesdaghi, Mehrnaz
- Khoddami, Maliheh
- Segarra-Roca, Anna
- Frohne, Alexandra
- Dmytrus, Jasmin
- Keramatipour, Mohammad
- Mansouri, Mahboubeh
- Eslamian, Golnaz
- Fallah, Shahrzad
- Boztug, Kaan
- Chavoshzadeh, Zahra
- SpringerLink (Online service)
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