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

Pons, R; Kekou, Kyriaki; Gkika, Artemis; Vogiatzakis, N.; Svigou, M; Papadimas, George K.; Youroukos, Sotiris; Kanavakis, M

doi:10.1016/s1090-3798(13)70474-4

European Journal of Paediatric Neurology

2013

DOI: 10.1016/s1090-3798(13)70474-4

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

R Pons¹,

Kyriaki Kekou²,

Artemis Gkika³

et al.

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

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