Missense variants in NDD-associated FBXO11 impair its localization and Fbxo11 deficiency leads to neuronal impairment in Drosophila melanogaster

Gregor A, Meerbrei T, Distel L, Gerstner T, Gupta A, Toutain A, Lynch SA, Maxton C, Lemke JR, Bernat JA, Bombei HM, Foulds N, Kuechler A, Bouman A, Bralo MP, Simarro FS, Garcia-Minaur S, Zweier C (2020)


Publication Type: Conference contribution

Publication year: 2020

Journal

Publisher: SPRINGERNATURE

City/Town: LONDON

Pages Range: 353-354

Conference Proceedings Title: EUROPEAN JOURNAL OF HUMAN GENETICS

Authors with CRIS profile

Involved external institutions

How to cite

APA:

Gregor, A., Meerbrei, T., Distel, L., Gerstner, T., Gupta, A., Toutain, A.,... Zweier, C. (2020). Missense variants in NDD-associated FBXO11 impair its localization and Fbxo11 deficiency leads to neuronal impairment in Drosophila melanogaster. In EUROPEAN JOURNAL OF HUMAN GENETICS (pp. 353-354). LONDON: SPRINGERNATURE.

MLA:

Gregor, Anne, et al. "Missense variants in NDD-associated FBXO11 impair its localization and Fbxo11 deficiency leads to neuronal impairment in Drosophila melanogaster." Proceedings of the EUROPEAN JOURNAL OF HUMAN GENETICS LONDON: SPRINGERNATURE, 2020. 353-354.

BibTeX: Download