Evidence of a Recessively Inherited CCN3 Mutation as a Rare...

Frontiers in Neurology 2020 / 5 Vol. 11

Evidence of a Recessively Inherited CCN3 Mutation as a Rare Cause of Early-Onset Parkinsonism

Bentley, Steven R., Khan, Suliman, Öchsner, Marco, Premarathne, Susitha, Aslam, Zain, Fowdar, Javed Y., Iqbal, Jamila, Naeem, Muhammad, Love, Christopher A., Wood, Stephen A., Mellick, George D., Syk
How much do you like this book?
What’s the quality of the file?
Download the book for quality assessment
What’s the quality of the downloaded files?
Volume:
11
Journal:
Frontiers in Neurology
DOI:
10.3389/fneur.2020.00331
Date:
May, 2020
File:
PDF, 732 KB
2020
Conversion to is in progress
Conversion to is failed