Prenatal diagnosis of Duchenne muscular dystrophy revealed a novel mosaic mutation in Dystrophin gene: a case report
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2350
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Prenatal diagnosis of Duchenne muscular dystrophy revealed a novel mosaic mutation in Dystrophin gene: a case report ; volume:21 ; number:1 ; day:11 ; month:11 ; year:2020 ; pages:1-10 ; date:12.2020
BMC medical genetics ; 21, Heft 1 (11.11.2020), 1-10, 12.2020
- Creator
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Wang, Yan
Chen, Yuhan
Wang, San Mei
Liu, Xin
Gu, Ya Nan
Feng, Zhichun
- Contributor
-
SpringerLink (Online service)
- DOI
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10.1186/s12881-020-01157-0
- URN
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urn:nbn:de:101:1-2020122219284568400021
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:21 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
- Wang, Yan
- Chen, Yuhan
- Wang, San Mei
- Liu, Xin
- Gu, Ya Nan
- Feng, Zhichun
- SpringerLink (Online service)
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Dystrophin Expressing Chimeric (DEC) Human Cells Provide a Potential Therapy for Duchenne Muscular Dystrophy
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Dystrophin Dp71 and the Neuropathophysiology of Duchenne Muscular Dystrophy
Dual exon skipping in myostatin and dystrophin for Duchenne muscular dystrophy
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Survival in Duchenne muscular dystrophy
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Deletion pattern in the dystrophin gene in Duchenne muscular dystrophy patients in northeast India
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Targeting angiogenesis in Duchenne muscular dystrophy
Pain characterization in Duchenne muscular dystrophy
Cognition trajectory in Duchenne muscular dystrophy
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