DOI:
10.1055/s-00000071
Seminars in Neurology
LinksClose Window
References
Dick KJ, Eckhardt M, Paisán-Ruiz C , et al.
Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35).
Hum Mutat 2010;
31 (4) E1251-E1260
We do not assume any responsibility for the contents of the web pages of other providers.