CHCHD10 mutations are not a common cause of SMN1-negative type III/IV spinal motor atrophy Reply




Jokela M, Penttila S, Udd B

PublisherWILEY-BLACKWELL

2015

Annals of Neurology

ANNALS OF NEUROLOGY

ANN NEUROL

78

5

831

832

2

0364-5134

1531-8249

DOIhttps://doi.org/10.1002/ana.24465




Last updated on 2024-26-11 at 13:59