Free Access
| Issue |
Med Sci (Paris)
Volume 31, Novembre 2015
Les Cahiers de Myologie
|
|
|---|---|---|
| Page(s) | 28 - 29 | |
| Section | Lu pour vous | |
| DOI | https://doi.org/10.1051/medsci/201531s307 | |
| Published online | 06 November 2015 | |
- Dusl M, Senderek J, Müller JS, Vogel JG, Pertl A, Stucka R, Lochmüller H, David R, Abicht A. A 3’-UTR mutation creates a microRNA target site in the GFPT1 gene of patients with congenital myasthenic syndrome. Hum Mol Genet 2015 ; 24 : 3418–3426. [CrossRef] [PubMed] [Google Scholar]
- Ceyhan-Birsoy O, Talim B, Swanson LC, Karakaya M, Graff MA, Beggs AH, Topaloglu H. Whole exome sequencing reveals DYSF, FKTN, and ISPD mutations in congenital muscular dystrophy without brain or eye involvement. J Neuromuscul Dis 2015 ; 2 : 87–92. [PubMed] [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.