- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource, 1 online resource.
- Language
-
Englisch
- Bibliographic citation
-
Immunodeficiency due to a novel variant in PIK3CD: a case report ; volume:21 ; number:1 ; day:20 ; month:7 ; year:2023 ; pages:1-5 ; date:12.2023
Pediatric rheumatology ; 21, Heft 1 (20.7.2023), 1-5, 12.2023
- Creator
-
Shashaani, Niloofar
Chavoshzadeh, Zahra
Ghasemi, Leila
Ghotbabadi, Shabnam Hajiani
Shiari, Sara
Sharafian, Samin
Shiari, Reza
- Contributor
-
SpringerLink (Online service)
- DOI
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10.1186/s12969-023-00859-y
- URN
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urn:nbn:de:101:1-2023102516095941476734
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 11:02 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Shashaani, Niloofar
- Chavoshzadeh, Zahra
- Ghasemi, Leila
- Ghotbabadi, Shabnam Hajiani
- Shiari, Sara
- Sharafian, Samin
- Shiari, Reza
- SpringerLink (Online service)
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First case report of infection due to Cupriavidus gilardii in a patient without immunodeficiency: a case report
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Expanding the phenotype of hypomaturation amelogenesis imperfecta due to a novel SLC24A4 variant
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A novel NFKB1 variant in a Japanese pedigree with common variable immunodeficiency
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A variant of RAG1 gene identified in severe combined immunodeficiency: a case report
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Spondylocarpotarsal synostosis syndrome due to a novel loss of function FLNB variant: a case report
First case report of infection due to Cupriavidus gilardii in a patient without immunodeficiency: a case report
Gastrointestinal Variant of Lemierre Syndrome due to Fusobacterium nucleatum: A Case Report
A novel 268 kb deletion combined with a splicing variant in IL7R causes of severe combined immunodeficiency in a Chinese family: a case report
Recurrent Nonimmune Fetal Hydrops Due to a Novel Pathogenic Variant in PIEZO1 Gene: A Case Report from South India
Expanding the phenotype of hypomaturation amelogenesis imperfecta due to a novel SLC24A4 variant
Expanding the phenotype of hypomaturation amelogenesis imperfecta due to a novel SLC24A4 variant