Opportunities and challenges for identifying undiagnosed Rare Disease patients through analysis of primary care records: long QT syndrome as a test case
- 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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Opportunities and challenges for identifying undiagnosed Rare Disease patients through analysis of primary care records: long QT syndrome as a test case ; volume:15 ; number:6 ; day:15 ; month:10 ; year:2024 ; pages:687-698 ; date:12.2024
Journal of community genetics ; 15, Heft 6 (15.10.2024), 687-698, 12.2024
- Urheber
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Evans, William
Akyea, Ralph K.
Simms, Alex
Kai, Joe
Qureshi, Nadeem
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1007/s12687-024-00742-7
- URN
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urn:nbn:de:101:1-2502252136404.601372983352
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 07:20 MESZ
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Beteiligte
- Evans, William
- Akyea, Ralph K.
- Simms, Alex
- Kai, Joe
- Qureshi, Nadeem
- SpringerLink (Online service)
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