- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
1 Online-Ressource.
- Language
-
Englisch
- Bibliographic citation
-
Monogenic lupus – from gene to targeted therapy ; volume:11 ; number:1 ; day:12 ; month:9 ; year:2024 ; pages:1-7 ; date:12.2024
Molecular and Cellular Pediatrics ; 11, Heft 1 (12.9.2024), 1-7, 12.2024
- Classification
-
Medizin, Gesundheit
- Creator
-
Menzel, Katharina
Novotna, Kateryna
Jeyakumar, Nivya
Wolf, Christine
Lee-Kirsch, Min Ae
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s40348-024-00181-x
- URN
-
urn:nbn:de:101:1-2411262101305.170924544086
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
- 15.08.2025, 7:28 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
- Menzel, Katharina
- Novotna, Kateryna
- Jeyakumar, Nivya
- Wolf, Christine
- Lee-Kirsch, Min Ae
- SpringerLink (Online service)
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Whole-genome sequencing identifies complex contributions to genetic risk by variants in genes causing monogenic systemic lupus erythematosus
Screening for extremely rare pathogenic variants of monogenic diabetes using targeted panel sequencing
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Correction to: LASSO‑derived nomogram for early identification of pediatric monogenic lupus
Familial Chilblain Lupus – A Monogenic Form of Cutaneous Lupus Erythematosus due to a Heterozygous Mutation in TREX1
Gene therapy for monogenic liver diseases: clinical successes, current challenges and future prospects
The monogenic signal
Impact of gene therapy for canine monogenic diseases on the progress of preclinical studies
Anti-interleukin-6 therapy through application of a monogenic protein inhibitor via gene delivery
Whole-genome sequencing identifies complex contributions to genetic risk by variants in genes causing monogenic systemic lupus erythematosus
Screening for extremely rare pathogenic variants of monogenic diabetes using targeted panel sequencing