Mutations in MYO9B are associated with Charcot-Marie-Tooth disease type 2 neuropathies and isolated optic atrophy
MYO9B 突变与 2 型腓骨肌萎缩症和孤立性视神经萎缩有关
期刊:European Journal of Neurology
影响因子:4.5
doi:10.1111/ene.15601
Silvia Cipriani, Marta Guerrero-Valero, Stefano Tozza, Edward Zhao, Veith Vollmer, Danique Beijer, Matt Danzi, Cristina Rivellini, Dejan Lazarevic, Giovanni Battista Pipitone, Bianca Rose Grosz, Costanza Lamperti, Stefania Bianchi Marzoli, Paola Carrera, Marcella Devoto, Chiara Pisciotta, Davide Par
神经
心力衰竭
肌萎缩症
FCM
IF
IHC-P
WB
PO4F1
