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Limb-girdle muscular dystrophy due to a novel homozygous ISPD gene mutation disclosed by whole exome sequencing
Mastorodemos, V., Vogiatzi, E., Latsoudis, H., Vorgia, P., Amoiridis, G., Zaganas, I.Volume:
357
Language:
english
Journal:
Journal of the Neurological Sciences
DOI:
10.1016/j.jns.2015.08.1205
Date:
October, 2015
File:
PDF, 51 KB
english, 2015