O.18 Systematic identification of causal mutations in...

Neuromuscular Disorders 2013 / 10 Vol. 23; Iss. 9-10

O.18 Systematic identification of causal mutations in Mendelian disorders using exome sequence data

Lek, M., Clarke, N.F., Waddell, L., Thomas, B., DePristo, M., Daly, M.J., North, K.N., MacArthur, D.G.
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Volume:
23
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2013.06.728
Date:
October, 2013
File:
PDF, 48 KB
english, 2013
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