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Montfrans, J.M. van; Hartman, E.A.R.; Braun, K.P.J.; Hennekam, E.A.M.; Hak, E.A.; Nederkoorn, P.J.; ... ; Gijn, M.E. van
2016
Phenotypic variability in patients with ADA2 deficiency due to identical homozygous R169Q mutations
Article / Letter to editor
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Es, M.A. van; Schelhaas, H.J.; Vught, P.W.J. van; Ticozzi, N.; Andersen, P.M.; Groen, E.J.N.; ... ; Berg, L.H. van den
2011
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
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