Free Access
Review
| Issue |
Med Sci (Paris)
Volume 33, Novembre 2017
Les Cahiers de Myologie
|
|
|---|---|---|
| Page(s) | 57 - 57 | |
| Section | Lu pour vous | |
| DOI | https://doi.org/10.1051/medsci/201733s112 | |
| Published online | 15 November 2017 | |
- Lefeber DJ, Xu L, Lek M, et al. A homozygous DPM3 mutation in a patient with alpha-dystroglycan-related limb girdle muscular dystrophy. Neuromuscular Disord 2017; Jul 17. pii: S0960–8966(17)30436–4. [Google Scholar]
- Bouchet-Séraphin C, Chelbi-Viallon M, Vuillaumier-Barrot S, Seta N. Gènes impliqués dans les alpha-dystroglycanopathies. Med Sci (Paris) 2016 ; 32 (hs2) : 40–45. [Google Scholar]
- Johnson K, Bertoli M, Phillips L, et al. The MYO-SEQ project: application of exome sequencing technologies to 1000 patients affected by limb-girdle weakness of unknown origin. Neuromuscular Disord 2016 ; 26 : S161. [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.