Assessment of the feasibility of exon 45–55 multiexon skipping for duchenne muscular dystrophy
- 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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Assessment of the feasibility of exon 45–55 multiexon skipping for duchenne muscular dystrophy ; volume:9 ; number:1 ; day:01 ; month:12 ; year:2008 ; pages:1-7 ; date:12.2008
BMC medical genetics ; 9, Heft 1 (01.12.2008), 1-7, 12.2008
- Creator
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van Vliet, Laura
- Contributor
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de Winter, Christa L.
van Deutekom, Judith CT
van Ommen, Gert-Jan B.
Aartsma-Rus, Annemieke
SpringerLink (Online service)
- DOI
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10.1186/1471-2350-9-105
- URN
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urn:nbn:de:1111-2016021834627
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:22 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
- van Vliet, Laura
- de Winter, Christa L.
- van Deutekom, Judith CT
- van Ommen, Gert-Jan B.
- Aartsma-Rus, Annemieke
- SpringerLink (Online service)
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Applying Lessons Learned from Developing Exon Skipping for Duchenne to Developing Individualized Exon Skipping Therapy for Patients with Neurodegenerative Diseases
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Adenine base editing-mediated exon skipping restores dystrophin in humanized Duchenne mouse model
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Exon skipping induced by nonsense/frameshift mutations in DMD gene results in Becker muscular dystrophy
Survival in Duchenne muscular dystrophy
Elevated nuclear TDP-43 induces constitutive exon skipping
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Applying Lessons Learned from Developing Exon Skipping for Duchenne to Developing Individualized Exon Skipping Therapy for Patients with Neurodegenerative Diseases
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Adenine base editing-mediated exon skipping restores dystrophin in humanized Duchenne mouse model
The dilemma of choice for duchenne patients eligible for Exon 51 skipping the European experience
Exon skipping induced by nonsense/frameshift mutations in DMD gene results in Becker muscular dystrophy
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Elevated nuclear TDP-43 induces constitutive exon skipping
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