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Browsing by Author Ngu, L.H.
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| Full Text | Issue Date | Title | Author(s) | | 2010 | Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiency. | Brun, L.; Ngu, L.H.; Keng, W.T.; Ch'ng, G.S.; Choy, Y.S., et al |
| 2009 | OFD1 is mutated in X-linked Joubert syndrome and interacts with LCA5-encoded lebercilin. | Coene, K.L.M.; Roepman, R.; Doherty, D.; Afroze, B.; Kroes, H.Y., et al |
Showing results 1 to 2 of 2
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