Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation
Chinnery, P. F., Crompton, D. E., Birchall, D., Jackson, M. J., Coulthard, A., Lombes, A., Quinn, N., Wills, A., Fletcher, N., Mottershead, J. P., Cooper, P., Kellett, M., Bates, D., Burn, J.Volume:
130
Language:
english
Journal:
Brain
DOI:
10.1093/brain/awl319
Date:
November, 2006
File:
PDF, 440 KB
english, 2006