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A novel mutation in PIEZO2 in a family presenting with autosomal dominant myopathy, ptosis, external ophthalmoplegia and distal symphalangism
Bertoli, M., Topf, A., Harris, E., Laval, S., Sarkozy, A., Lochmüller, H., Lynch, S., Straub, V.Volume:
25
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2015.06.327
Date:
October, 2015
File:
PDF, 222 KB
english, 2015