Published in
Wiley, European Journal of Neurology, 3(25), p. 602-605, 2018
DOI: 10.1111/ene.13557
Elsevier, Journal of the Neurological Sciences, (405), p. 89, 2019
DOI: 10.1016/j.jns.2019.10.1731
Links
Tools
Severe 5,10-methylenetetrahydrofolate reductase deficiency: a rare, treatable cause of complicated hereditary spastic paraplegia
Journal article published in 2018 by
A. Perna,
D. Dave,
M. Masciullo 
,
F. Khan,
A. Modoni,
E. Cellini,
S. Rohatgi,
E. Parrini,
S. Nirhale,
E. Ricci,
P. Rao,
G. Silvestri ,
A. M. Donati,
P. Naphade
,
F. Khan,
A. Modoni,
E. Cellini,
S. Rohatgi,
E. Parrini,
S. Nirhale,
E. Ricci,
P. Rao,
G. Silvestri ,
A. M. Donati,
P. Naphade
This paper is made freely available by the publisher.
Full text: Download
Published version:
archiving forbidden
Data provided by 