Distinct clinical phenotypes in a family with a novel truncating MEN1 frameshift mutation
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1472-6823
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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Distinct clinical phenotypes in a family with a novel truncating MEN1 frameshift mutation ; volume:22 ; number:1 ; day:14 ; month:3 ; year:2022 ; pages:1-8 ; date:12.2022
BMC endocrine disorders ; 22, Heft 1 (14.3.2022), 1-8, 12.2022
- Urheber
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Welsch, Christoph
Flügel, Anna Katharina
Rondot, Susanne
Schulze, Egbert
Sircar, Ishani
Nußbaumer, Judith
Bojunga, Jörg
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1186/s12902-022-00978-9
- URN
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urn:nbn:de:101:1-2022060701264717216681
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:26 MESZ
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Beteiligte
- Welsch, Christoph
- Flügel, Anna Katharina
- Rondot, Susanne
- Schulze, Egbert
- Sircar, Ishani
- Nußbaumer, Judith
- Bojunga, Jörg
- SpringerLink (Online service)
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