G.O.4 - Autosomal recessive mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita
| Autor: | Ravenscroft, G., Nolent, F., Rajagopalan, S., Meireles, A., Paavola, K., Gaillard, D., Alanio, E., Buckland, M., Arbuckle, S., Krivanek, M., Maluenda, J., Pannell, S., Gooding, R., Ong, R., Allcock, R., Kok, F., Talbot, W., Melki, J., Laing, N. * |
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| Zdroj: | In Neuromuscular Disorders October 2015 25 Supplement 2:S186-S186 |
| Databáze: | ScienceDirect |
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