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Browsing by Author Fischer, B.
Showing results 1 to 4 of 4
| Full Text | Issue Date | Title | Author(s) | | 2011 | NOA1 is an essential GTPase required for mitochondrial protein synthesis. | Kolanczyk, M.; Pech, M.; Zemojtel, T.; Yamamoto, H.; Mikula, I., et al |
| 2009 | Vacuolar H+-ATPase meets glycosylation in patients with cutis laxa. | Guillard, M.; Dimopoulou, A.; Fischer, B.; Morava, E.; Lefeber, D.J., et al |
| 2009 | Loss-of-function mutations in ATP6V0A2 impair vesicular trafficking, tropoelastin secretion and cell survival. | Hucthagowder, V.; Morava, E.; Kornak, U.; Lefeber, D.J.; Fischer, B., et al |
| 2008 | Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2. | Kornak, U.; Reynders, E.; Dimopoulou, A.; Reeuwijk, J. van; Fischer, B., et al |
Showing results 1 to 4 of 4
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