Multilevel molecular analysis identifies all dystrophin...

Neuromuscular Disorders 2017 / 10 Vol. 27

Multilevel molecular analysis identifies all dystrophin gene mutations pointing out that DMD is a genetically homogenous disease: repercussions on diagnosis, prevention and therapy

Neri, M., Selvatici, R., Falzarano, M., Trabanelli, C., Ravani, A., Rimessi, P., Fabris, M., Scotton, C., Mauro, A., Fortunato, F., Osman, H., Rossi, R., Armaroli, A., Buldrini, B., Fini, S., Gualandi
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:
27
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2017.06.377
Date:
October, 2017
File:
PDF, 228 KB
english, 2017
Conversion to is in progress
Conversion to is failed