DOI:
10.1055/s-00000041
Neuropediatrics
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References
Donger C, Krejci E, Serradell AP, Eymard B, Bon S, Nicole S. et al.
Mutation in the human acetylcholinesterase-associated collagen gene, COLQ, is responsible for congenital myasthenic syndrome with end-plate acetylcholinesterase deficiency (Type Ic).
Am J Hum Genet 1998; 63: 967-975
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