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

Parkinsonism Relat Disord

IRCCS Foundation Ca' Granda Ospedale Maggiore Policlinico, Dino Ferrari Center, Neuroscience Section, Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy. Electronic address:

Published: March 2018

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.parkreldis.2017.12.025DOI Listing

Publication Analysis

Top Keywords

novo c19orf12
4
c19orf12 heterozygous
4
heterozygous mutation
4
mutation patient
4
patient mpan
4
novo
1
heterozygous
1
mutation
1
patient
1
mpan
1

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!