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Browsing by Author Spiekerkotter, U.

Full Text	Issue Date	Title	Author(s)
	2010	Novel mutations in the NDUFS1 gene cause low residual activities in human complex I deficiencies.	Hoefs, S.J.G.; Skjeldal, O.H.; Rodenburg, R.J.T.; Nedregaard, B.; Kaauwen, E. van, et al
	2007	Cystic renal dysplasia as a leading sign of inherited metabolic disease.	Distelmaier, F.; Vogel, M.; Spiekerkotter, U.; Gempel, K.; Klee, D., et al