Hochschulschrift

Gene therapy for muscular dystrophy using secondary modifiers of the dystrophic phenotype

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Notes: Regensburg, Univ., Diss., 2004

Keyword: Gentherapie ; Muskeldystrophie ; Duchenne-Syndrom
Histologie
Cytologie

Creator: Abmayr, Simone

URN: urn:nbn:de:bvb:355-opus-4086

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:31 AM CEST

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Abmayr, Simone

Other Objects (12)

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Gene therapy for muscular dystrophy using secondary modifiers of the dystrophic phenotype

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Other Objects (12)

Gene therapy for muscular dystrophy using secondary modifiers of the dystrophic phenotype

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Pannexin 1 dysregulation in Duchenne muscular dystrophy and its exacerbation of dystrophic features in mdx mice

Macroglossia and less advanced dystrophic change in the tongue muscle of the Duchenne muscular dystrophy rat

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Dystrophic epidermolysis bullosa: secondary disease mechanisms and disease modifiers

Pannexin 1 dysregulation in Duchenne muscular dystrophy and its exacerbation of dystrophic features in mdx mice

Macroglossia and less advanced dystrophic change in the tongue muscle of the Duchenne muscular dystrophy rat

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Genome-wide association study to identify potential genetic modifiers in a canine model for Duchenne muscular dystrophy

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Macroglossia and less advanced dystrophic change in the tongue muscle of the Duchenne muscular dystrophy rat

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