J. COLOMER Et Al. , "Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2," NEUROMUSCULAR DISORDERS , vol.16, no.7, pp.449-453, 2006
COLOMER, J. Et Al. 2006. Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2. NEUROMUSCULAR DISORDERS , vol.16, no.7 , 449-453.
COLOMER, J., GOODING, R., ANGELICHEVA, D., KING, R. H. M., GUILLEN-NAVARRO, E., Parman, Y., ... NASCIMENTO, A.(2006). Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2. NEUROMUSCULAR DISORDERS , vol.16, no.7, 449-453.
COLOMER, Jaume Et Al. "Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2," NEUROMUSCULAR DISORDERS , vol.16, no.7, 449-453, 2006
COLOMER, Jaume Et Al. "Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2." NEUROMUSCULAR DISORDERS , vol.16, no.7, pp.449-453, 2006
COLOMER, J. Et Al. (2006) . "Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2." NEUROMUSCULAR DISORDERS , vol.16, no.7, pp.449-453.
@article{article, author={Jaume COLOMER Et Al. }, title={Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2}, journal={NEUROMUSCULAR DISORDERS}, year=2006, pages={449-453} }