![](/img/cover-not-exists.png)
Autosomal recessive mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita
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, RVolume:
25
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2015.06.013
Date:
October, 2015
File:
PDF, 206 KB
english, 2015