Opportunities and challenges for identifying undiagnosed Rare Disease patients through analysis of primary care records: long QT syndrome as a test case
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
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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
- Creator
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Evans, William
Akyea, Ralph K.
Simms, Alex
Kai, Joe
Qureshi, Nadeem
- Contributor
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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
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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19.04.20242031, 2:05 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
- Evans, William
- Akyea, Ralph K.
- Simms, Alex
- Kai, Joe
- Qureshi, Nadeem
- SpringerLink (Online service)
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