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Kuechler, A.* ; Fritzen, D.* ; Becker, J.* ; Peters, S.* ; Sturm, M.* ; Hundertmark, H.* ; Schmidt, A.* ; Kreiss, M.* ; Strom, T.M. ; Wieczorek, D.* ; Haack, T.* ; Beck-Woedl, S.* ; Cremer, K.* ; Engels, H.*

De novo FBXO11 mutations are associated with intellectual disability, microcephaly and behavioural anomalies.

Eur. J. Hum. Genet. 27, 228-229 (2019)

Open Access Green as soon as Postprint is submitted to ZB.

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Publication type Article: Journal article

Document type Meeting abstract

Corresponding Author

ISSN (print) / ISBN 1018-4813

e-ISSN 1476-5438

Journal European Journal of Human Genetics

Quellenangaben Volume: 27, Pages: 228-229

Publisher Nature Publishing Group

Publishing Place Macmillan Building, 4 Crinan St, London N1 9xw, England

Non-patent literature Publications

Reviewing status Peer reviewed

Institute(s) Institute of Human Genetics (IHG)