Mice with an autosomal dominant Charcot-Marie-Tooth type 2O disease mutation in both dynein alleles display severe moto-sensory phenotypes

por Nandini, Swaran, Conley Calderon, Jami L., Sabblah, Thywill T., Love, Rachal, King, Linda E., King, Stephen J.
Publicado 2019

A novel mouse model carrying a human cytoplasmic dynein mutation shows motor behavior deficits consistent with Charcot-Marie-Tooth type 2O disease

por Sabblah, Thywill T., Nandini, Swaran, Ledray, Aaron P., Pasos, Julio, Calderon, Jami L. Conley, Love, Rachal, King, Linda E., King, Stephen J.
Publicado 2018