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A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation
Fogli, A., Dionisi-Vici, C., Deodato, F., Bartuli, A., Boespflug-Tanguy, O., Bertini, E.Volume:
59
Language:
english
Journal:
Neurology
DOI:
10.1212/01.WNL.0000041666.76863.47
Date:
December, 2002
File:
PDF, 244 KB
english, 2002