G.P.2 Mutations in the human isoprenoid synthase domain...

Neuromuscular Disorders 2012 / 10 Vol. 22; Iss. 9-10

G.P.2 Mutations in the human isoprenoid synthase domain containing gene are a common cause of congenital and limb girdle muscular dystrophies

Cirak, S., Foley, R.A., Herrmann, R., Willer, T., Elisabeth, S., Yau, M., Brodd, L., Torelli, S., Kamynina, A., Vondracek, P., Roper, H., Longman, C., Korinthenberg, R., Marrosu, G., Nurnberg, P., Pla
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Volume:
22
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2012.06.036
Date:
October, 2012
File:
PDF, 52 KB
english, 2012
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