Rare and potential pathogenic mutations of LMNA and LAMA4 associated with familial arrhythmogenic right ventricular cardiomyopathy/dysplasia with right ventricular heart failure, cerebral thromboembolism and hereditary electrocardiogram abnormality
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1750-1172
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Rare and potential pathogenic mutations of LMNA and LAMA4 associated with familial arrhythmogenic right ventricular cardiomyopathy/dysplasia with right ventricular heart failure, cerebral thromboembolism and hereditary electrocardiogram abnormality ; volume:17 ; number:1 ; day:7 ; month:5 ; year:2022 ; pages:1-17 ; date:12.2022
Orphanet journal of rare diseases ; 17, Heft 1 (7.5.2022), 1-17, 12.2022
- Creator
-
Chen, Jia
Ma, Yuting
Li, Hong
Lin, Zhuo
Yang, Zhe
Zhang, Qin
Wang, Feng
Lin, Yanping
Ye, Zebing
Lin, Yubi
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s13023-022-02348-z
- URN
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urn:nbn:de:101:1-2022071520311168558145
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:33 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Chen, Jia
- Ma, Yuting
- Li, Hong
- Lin, Zhuo
- Yang, Zhe
- Zhang, Qin
- Wang, Feng
- Lin, Yanping
- Ye, Zebing
- Lin, Yubi
- SpringerLink (Online service)
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Ablation of ventricular tachycardia in arrhythmogenic right ventricular dysplasia/cardiomyopathy
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