Expanded King–Denborough phenotype and congenital myopathy in two brothers with RYR1 mutation
Munell, F., Sanchez-Montáñez, A., Quijano-Roy, S., Gratacos, M., Martinez-Saez, E., Ferrer Aparicio, S., Gomez Garcia de la Banda, M., Urreizti, R., Grinberg, D.Volume:
26
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2016.06.183
Date:
October, 2016
File:
PDF, 192 KB
english, 2016