Autosomal recessive mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita
G. Ravenscroft F Nolent; S Rajagopalan; A Meireles; K Paavola; D Gaillard; E Alanio; M Buckland; S Arbuckle; M Krivanek; J Maluenda; S Pannell; R Gooding; R Ong; R Allcock; F Kok; W Talbot; J Melki; N Laing; International Congress of the World Muscle Society (20. 2015 Brighton)
Neuromuscular Disorders London v. 25, suppl. 2, p. S186, res. G.O.4, 2015
London 2015
Localização:
FM - Fac. Medicina
(BCSEP 271 2015 )(Acessar)