Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations

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Publication year
2020
Author(s)
Connaughton, D.M.
Dai, R.
Owen, D.J.
Marquez, J.
Mann, N.
Graham-Paquin, A.L.
Nakayama, M.
Coyaud, E.
Laurent, E.M.N.
St-Germain, J.R.
Snijders-Blok, L.
Vino, A.
Klämbt, V.
Deutsch, K.
Wu, C.H.W.
Kolvenbach, C.M.
Kause, F.
Ottlewski, I.
Schneider, R.
Kitzler, T.M.
Majmundar, A.J.
Buerger, F.
Onuchic-Whitford, A.C.
Youying, M.
Kolb, A.
Salmanullah, D.
Chen, E.
Ven, A.T. van der
Rao, J.
Ityel, H.
Seltzsam, S.
Rieke, J.M.
Chen, J.
Vivante, A.
Hwang, D.Y.
Kohl, S.
Dworschak, G.C.
Hermle, T.
Alders, M.
Bartolomaeus, T.
Bauer, S.T.
Baum, M.A.
Brilstra, E.H.
Challman, T.D.
Zyskind, J.
Costin, C.E.
Dipple, K.M.
Duijkers, F.A.
Ferguson, M.
Fitzpatrick, D.R.
Fick, R.
Glass, I.A.
Hulick, P.J.
Kline, A.D.
Krey, I.
Kumar, S.
Lu, W.
Marco, E.J.
Wentzensen, I.M.
Fisher, S.E.
Bouchard, M.
Khokha, M.K.
Shril, S.
Hildebrandt, F.
Source
American Journal of Human Genetics, 107, 4, (2020), pp. 727-742
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DOI
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/229002   https://hdl.handle.net/2066/229002
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