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P295 – 1801 A single aminoacid deletion in the dystrophin protein associated with a mild clinical phenotype.

Authors :
Pons, R
Kekou, K
Gkika, A
Vogiatzakis, N
Svigou, M
Papadimas, G
Youroukos, S
Kanavakis, M
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