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The spectrum of mutations that underlie the neuromuscular junction synaptopathy in DOK7 congenital myasthenic syndrome
Cossins, J., Liu, W. W., Belaya, K., Maxwell, S., Oldridge, M., Lester, T., Robb, S., Beeson, D.Volume:
21
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/dds198
Date:
September, 2012
File:
PDF, 561 KB
english, 2012