De novo REEP2 missense mutation in pure hereditary spastic paraplegia.

Autor: Roda, Ricardo H.1,2 rroda1@jhmi.edu, Schindler, Alice B.2, Blackstone, Craig2
Zdroj: Annals of Clinical & Translational Neurology. May2017, Vol. 4 Issue 5, p347-350. 4p.
Databáze: Academic Search Ultimate