Skeletal muscle cell protein dysregulation highlights the pathogenesis mechanism of myopathy-associated p97/VCP R155H mutations.
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| Title: | Skeletal muscle cell protein dysregulation highlights the pathogenesis mechanism of myopathy-associated p97/VCP R155H mutations. |
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| Authors: | Luzzi A; The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, United States., Wang F; The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, United States., Li S; The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, United States., Iacovino M; The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, United States.; Department of Pediatrics, David Geffen School of Medicine at UCLA, Los Angeles, CA, United States., Chou TF; The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, United States.; Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, United States. |
| Source: | Frontiers in neurology [Front Neurol] 2023 Aug 03; Vol. 14, pp. 1211635. Date of Electronic Publication: 2023 Aug 03 (Print Publication: 2023). |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101546899 Publication Model: eCollection Cited Medium: Print ISSN: 1664-2295 (Print) Linking ISSN: 16642295 NLM ISO Abbreviation: Front Neurol Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
| ISSN: | 1664-2295 |
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| DOI: | 10.3389/fneur.2023.1211635 |
