Erschienen in:

01.06.2008 | LETTER TO THE EDITORS

Extending the clinical spectrum of SPG3A mutations to a very severe and very early complicated phenotype

verfasst von: J. Haberlová, MD, K. G. Claeys, MD, PhD, J. Zámečník, MD, PhD, P. De Jonghe, MD, PhD, P. Seeman, MD, PhD

Erschienen in: Journal of Neurology | Ausgabe 6/2008