The first Turkish family with the diagnosis of retinal vasculopathy with cerebral leukodystrophy (RVCL) where a new mutation was found

Autor: Bademkiran, F., Nalcaci, S., Eraslan, C., Durmaz, A.
Zdroj: In Journal of the Neurological Sciences 15 October 2017 381 Supplement:378-379
Databáze: ScienceDirect