DOI:
10.1055/s-00000071
Seminars in Neurology
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References
Alazami AM, Adly N, Al Dhalaan H, Alkuraya FS.
A nullimorphic ERLIN2 mutation defines a complicated hereditary spastic paraplegia locus (SPG18).
Neurogenetics 2011;
12 (4) 333-336
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