E. Storey
P.146 Characterising the molecular consequences of LMNA-related congenital muscular dystrophy in patient myoblasts
Storey, E.; Holt, I.; Owen, S.; Synowsky, S.; Shirran, S.; Morris, G.; Fuller, H.
Authors
I. Holt
Sharon Owen s.j.owen@keele.ac.uk
S. Synowsky
S. Shirran
G. Morris
Heidi Fuller h.r.fuller@keele.ac.uk
| Journal Article Type | Article |
|---|---|
| Acceptance Date | Oct 1, 2022 |
| Publication Date | 2022-10 |
| Deposit Date | Jun 1, 2023 |
| Journal | Neuromuscular Disorders |
| Print ISSN | 0960-8966 |
| Publisher | Elsevier |
| Peer Reviewed | Peer Reviewed |
| Volume | 32 |
| Pages | S108 |
| DOI | https://doi.org/10.1016/j.nmd.2022.07.274 |
| Keywords | Genetics (clinical); Neurology (clinical); Neurology; Pediatrics, Perinatology and Child Health |
| Additional Information | This article is maintained by: Elsevier; Article Title: P.146 Characterising the molecular consequences of LMNA-related congenital muscular dystrophy in patient myoblasts; Journal Title: Neuromuscular Disorders; CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.nmd.2022.07.274; Content Type: simple-article; Copyright: Copyright © 2022 Published by Elsevier B.V. |
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