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A de novo C19orf12 heterozygous mutation in a patient with MPAN.

Parkinsonism & related disorders - 1 Mar 2018

Monfrini Edoardo, Melzi Valentina, Buongarzone Gabriele, Franco Giulia, Ronchi Dario, Dilena Robertino, Scola Elisa, Vizziello Paola, Bordoni Andreina, Bresolin Nereo, Comi Giacomo Pietro, Corti Stefania, Di Fonzo Alessio

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PMID: 29295770
DOI: 10.1016/j.parkreldis.2017.12.025

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