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C.P.2 In silico analysis of recessive RYR1 mutations identifies novel potential disease mechanisms
Hwang, J.H., Amburgey, K., Treves, S., Zorzato, F., Dowling, J.J., Clarke, N.F.Volume:
22
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2012.06.130
Date:
October, 2012
File:
PDF, 46 KB
english, 2012