Emotional behavior and brain anatomy of the mdx52 mouse model of Duchenne muscular dystrophy

• Prif Awduron: Amel Saoudi (Awdur), Faouzi Zarrouki (Awdur), Catherine Sebrié (Awdur), Charlotte Izabelle (Awdur), Aurélie Goyenvalle (Awdur), Cyrille Vaillend (Awdur)
• Fformat: Llyfr
• Cyhoeddwyd: The Company of Biologists, 2021-09-01T00:00:00Z.
• Pynciau: article
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The exon-52-deleted mdx52 mouse is a critical model of Duchenne muscular dystrophy (DMD), as it features a deletion in a hotspot region of the DMD gene, frequently mutated in patients. Deletion of exon 52 impedes expression of several brain dystrophins (Dp427, Dp260 and Dp140), thus providing a key...