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Browsing by Author Kassubek, J.

Full Text	Issue Date	Title	Author(s)
	2008	REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31.	Beetz, C.; Schule, R.; Deconinck, T.; Tran-Viet, K.N.; Zhu, H., et al
	2008	SPG10 is a rare cause of spastic paraplegia in European families.	Schule, R.; Kremer, B.P.; Kassubek, J.; Auer-Grumbach, M.; Kostic, V., et al