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P295 – 1801 A single aminoacid deletion in the dystrophin protein associated with a mild clinical phenotype.
- Source :
- European Journal of Paediatric Neurology; Sep2013 Supplement, Vol. 17, pS135-S135, 1p
- Publication Year :
- 2013
Details
- Language :
- English
- ISSN :
- 10903798
- Volume :
- 17
- Database :
- Supplemental Index
- Journal :
- European Journal of Paediatric Neurology
- Publication Type :
- Academic Journal
- Accession number :
- 90277783
- Full Text :
- https://doi.org/10.1016/S1090-3798(13)70474-4