Free Access
Issue |
Med Sci (Paris)
Volume 37, Novembre 2021
Les Cahiers de Myologie
|
|
---|---|---|
Page(s) | 48 - 48 | |
Section | Lu pour Vous | |
DOI | https://doi.org/10.1051/medsci/2021193 | |
Published online | 08 December 2021 |
- Abath Neto OL, Medne L, Donkervoort S, et al. MLIP causes recessive myopathy with rhabdomyolysis, myalgia and baseline high serum creatine kinase. Brain 2021 Sep 28:awab275. doi: 10.1093/brain/awab275. [Google Scholar]
- Scalco RS, Gardiner AR, Pitceathly RD, et al. Rhabdomyolysis: a genetic perspective. Orphanet J Rare Dis 2015 ; 10 : 51. [CrossRef] [PubMed] [Google Scholar]
- Mezreani J, Martin F, Audet S, et al. Isoform specific variant in MLIP as a potential cause of adult-onset distal myopathy. Neuromuscul Dis 2021; 31 : S71. [CrossRef] [Google Scholar]
Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.
Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.
Initial download of the metrics may take a while.