المؤلفون: Vodopiutz, J. (Julia), Seidl, R. (Rainer), Prayer, D. (Daniela), Khan, M.I. (M. Imran), Mayr, J.A. (Johannes A.), Streubel, B. (Berthold), Steiß, J.-O. (Jens-Oliver), Hahn, A. (Andreas), Csaicsich, D. (Dagmar), Castro, C. (Christel), Assoum, M. (Mirna), Müller, T. (Thomas), Wieczorek, D. (Dagmar), Mancini, G.M.S. (Grazia), Sadowski, C.E. (Carolin E.), Lévy, N. (Nicolas), Megarbane, A. (Andre), Godbole, K. (Koumudi), Schanze, D. (Denny), Hildebrandt, F. (Friedhelm), Delague, V. (Valérie), Janecke, A.R. (Andreas), Zenker, M. (Martin)

المصدر: Human Mutation vol. 36 no. 11, pp. 1021-1028

مصطلحات موضوعية: Basal ganglia, Cerebellar atrophy, Galloway-Mowat, Intellectual disability, Optic atrophy, Retinopathy, SCAR5, WDR73

Relation: http://repub.eur.nl/pub/92233; urn:hdl:1765/92233

الاتاحة: http://repub.eur.nl/pub/92233
https://doi.org/10.1002/humu.22828