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Browsing by Author Sass, J.O.
Showing results 1 to 3 of 3
| Full Text | Issue Date | Title | Author(s) | | 2011 | Whole-exome sequencing detects somatic mutations of IDH1 in metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria (MC-HGA) | Vissers, L.E.L.M.; Fano, V.; Martinelli, D.; Campos-Xavier, B.; Barbuti, D., et al |
| 2008 | NMR spectroscopy of aminoacylase 1 deficiency, a novel inborn error of metabolism. | Engelke, U.F.H.; Sass, J.O.; Coster, R.N. van; Gerlo, E.; Olbrich, H., et al |
| 2006 | Mutations in ACY1, the gene encoding aminoacylase 1, cause a novel inborn error of metabolism. | Sass, J.O.; Mohr, V.; Olbrich, H.; Engelke, U.F.H.; Horvath, J., et al |
Showing results 1 to 3 of 3
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