PLEKHG5 deficiency leads to an intermediate form of...

Human Molecular Genetics 2013 / 10 Vol. 22; Iss. 20

PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot-Marie-Tooth disease

Azzedine, H., Zavadakova, P., Plante-Bordeneuve, V., Vaz Pato, M., Pinto, N., Bartesaghi, L., Zenker, J., Poirot, O., Bernard-Marissal, N., Arnaud Gouttenoire, E., Cartoni, R., Title, A., Venturini, G
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:
22
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/ddt274
Date:
October, 2013
File:
PDF, 1.29 MB
english, 2013
Conversion to is in progress
Conversion to is failed