Whole-exome sequencing revealed a likely pathogenic variant in NF1 causing neurofibromatosis type I and Arrhythmogenic Cardiomyopathy
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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1 Online-Ressource.
- Sprache
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Englisch
- Erschienen in
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Whole-exome sequencing revealed a likely pathogenic variant in NF1 causing neurofibromatosis type I and Arrhythmogenic Cardiomyopathy ; volume:24 ; number:1 ; day:23 ; month:4 ; year:2024 ; pages:1-6 ; date:12.2024
BMC cardiovascular disorders ; 24, Heft 1 (23.4.2024), 1-6, 12.2024
- Urheber
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Pourirahim, Maryam
Houshmand, Golnaz
Abdolkarimi, Leyla
Maleki, Majid
Kalayinia, Samira
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1186/s12872-024-03878-z
- URN
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urn:nbn:de:101:1-2407090912518.620091049332
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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14.08.2025, 11:01 MESZ
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Beteiligte
- Pourirahim, Maryam
- Houshmand, Golnaz
- Abdolkarimi, Leyla
- Maleki, Majid
- Kalayinia, Samira
- SpringerLink (Online service)
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