Broad clinical spectrum observed in patients with...

Neuromuscular Disorders 2017 / 10 Vol. 27

Broad clinical spectrum observed in patients with scapuloperoneal spinal muscular atrophy (SPSMA) caused by an c.806G > A (p. Arg269His) mutation in the TRPV4 gene

Jędrzejowska, M., Dębek, E., Halat, P., Kostera-Pruszczyk, A., Jezela-Stanek, A., Ciara, E., Rydzanicz, M., Gasperowicz, P., Gos, M.
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.2017.06.158
Date:
October, 2017
File:
PDF, 241 KB
english, 2017
Conversion to is in progress
Conversion to is failed