Foti FM

References (1)

Title : Severe congenital myasthenic syndrome associated with novel biallelic mutation of the CHRND gene - Bonanno_2020_Neuromuscul.Disord__
Author(s) : Bonanno C , Rodolico C , Topf A , Foti FM , Liu WW , Beeson D , Toscano A , Lochmuller H
Ref : Neuromuscular Disorders , : , 2020
Abstract : Bonanno_2020_Neuromuscul.Disord__
ESTHER : Bonanno_2020_Neuromuscul.Disord__
PubMedSearch : Bonanno_2020_Neuromuscul.Disord__
PubMedID: 32360402