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Browsing by Author Saada, A.

Full Text	Issue Date	Title	Author(s)
	2011	Mutation in mitochondrial ribosomal protein MRPS22 leads to Cornelia de Lange-like phenotype, brain abnormalities and hypertrophic cardiomyopathy	Smits, P.; Saada, A.; Wortmann, S.B.; Heister, A.; Brink, M., et al
	2009	Mutations in NDUFAF3 (C3ORF60), encoding an NDUFAF4 (C6ORF66)-interacting complex I assembly protein, cause fatal neonatal mitochondrial disease.	Saada, A.; Vogel, R.O.; Hoefs, S.J.G.; Brand, M.A.M. van den; Wessels, H.J., et al
	2006	Distinct clinical phenotypes associated with a mutation in the mitochondrial translation elongation factor EFTs.	Smeitink, J.A.M.; Elpeleg, O.N.; Antonicka, H.; Diepstra, H.D.; Saada, A., et al