A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2045-2322
- 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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A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A ; volume:9 ; number:1 ; day:27 ; month:2 ; year:2019 ; pages:1-12 ; date:12.2019
Scientific reports ; 9, Heft 1 (27.2.2019), 1-12, 12.2019
- Klassifikation
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Naturwissenschaften
- Urheber
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Demal, Till Joscha
Heise, Melina
Reiz, Benedikt
Dogra, Deepika
Brænne, Ingrid
Reichenspurner, Hermann
Männer, Jörg
Aherrahrou, Zouhair
Schunkert, Heribert
Erdmann, Jeanette
Seyfried, Salim
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1038/s41598-019-39648-7
- URN
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urn:nbn:de:101:1-2019031721145964131224
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:57 MESZ
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Beteiligte
- Demal, Till Joscha
- Heise, Melina
- Reiz, Benedikt
- Dogra, Deepika
- Brænne, Ingrid
- Reichenspurner, Hermann
- Männer, Jörg
- Aherrahrou, Zouhair
- Schunkert, Heribert
- Erdmann, Jeanette
- Seyfried, Salim
- SpringerLink (Online service)
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