Arenas Barbero, Joaquín Martín, Miguel Ángel Martinez Azorin, Francisco
Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene. [caso clínico] - Brain & development, 2016 - 38(1):167-72.
Formato Vancouver:
Castro Gago M, Dacruz Alvárez D, Pintos Martínez E, Beiras Iglesias A, Arenas J, Martín MÁ et al. Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene. Brain Dev. 2016 Jan;38(1):167-72.
PMID: 26006750
Contiene 20 referencias
Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene. [caso clínico] - Brain & development, 2016 - 38(1):167-72.
Formato Vancouver:
Castro Gago M, Dacruz Alvárez D, Pintos Martínez E, Beiras Iglesias A, Arenas J, Martín MÁ et al. Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene. Brain Dev. 2016 Jan;38(1):167-72.
PMID: 26006750
Contiene 20 referencias
