To the Editor We recently read the article by Caroppo et al1 with interest, and we congratulate them for their excellent work. Caroppo et al1 analyzed 19 families in which affected individuals presented with atypical parkinsonism and a progressive supranuclear palsy (PSP)–like phenotype. They also identified a DCTN1 G71E mutation in 4 of the affected patients; all were from a single French family. The mutation was reported previously in another French family.2
Fujioka S, Tacik P, Wszolek ZK. DCTN1 Mutations and Progressive Supranuclear Palsy–Like Phenotype. JAMA Neurol. 2014;71(5):655. doi:10.1001/jamaneurol.2014.227
Customize your JAMA Network experience by selecting one or more topics from the list below.
Create a personal account or sign in to: