De novo variants in MAPK8IP3 cause intellectual disability with variable brain anomalies

Platzer K, Sticht H, Edwards SL, Allen W, Angione KM, Bonati MT, Brasington C, Cho MT, Demmer LA, Falik-Zaccai T, Gamble CN, Hellenbroich Y, Iascone M, Kok F, Mahida S, Mandel H, Marquardt T, Mcwalter K, Panis B, Pepler A, Pinz H, Ramos L, Shinde DN, Smith-Hicks C, Stegmann APA, Stoebe P, Stumpel CTRM, Wilson C, Lemke JR, Di Donato N, Miller KG, Abou Jamra R (2019)

Publication Type: Conference contribution

Publication year: 2019

Journal

Publisher: NATURE PUBLISHING GROUP

City/Town: LONDON

Pages Range: 1117-1118

Conference Proceedings Title: EUROPEAN JOURNAL OF HUMAN GENETICS

Event location: Gothenburg, SWEDEN

DOI: 10.1016/j.ajhg.2018.12.008

Authors with CRIS profile

Involved external institutions

Oklahoma Medical Research Foundation (OMRF) United States (USA) (US) Carolinas HealthCare System United States (USA) (US) CeGaT GmbH Germany (DE) Zuyderland Medical Center Netherlands (NL) University of Colorado System United States (USA) (US) Universität zu Lübeck Germany (DE) Universität Leipzig Germany (DE) North Carolina Biotechnology Center United States (USA) (US) Saint Louis University (SLU) United States (USA) (US) Universitätsklinikum Münster Germany (DE) GeneDX United States (USA) (US) Maastricht University Netherlands (NL) Johns Hopkins University (JHU) United States (USA) (US) ASST Papa Giovanni XXIII Italy (IT) Galilee Medical Center / המרכז הרפואי לגליל Israel (IL) Ambry Genetics United States (USA) (US) Instituto Auxologico Italiano Italy (IT) Technische Universität Dresden Germany (DE) University of Texas Health Science Center at Houston (UTHealth) United States (USA) (US)

How to cite

APA:

Platzer, K., Sticht, H., Edwards, S.L., Allen, W., Angione, K.M., Bonati, M.T.,... Abou Jamra, R. (2019). De novo variants in MAPK8IP3 cause intellectual disability with variable brain anomalies. In EUROPEAN JOURNAL OF HUMAN GENETICS (pp. 1117-1118). Gothenburg, SWEDEN: LONDON: NATURE PUBLISHING GROUP.

MLA:

Platzer, K., et al. "De novo variants in MAPK8IP3 cause intellectual disability with variable brain anomalies." Proceedings of the 52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg, SWEDEN LONDON: NATURE PUBLISHING GROUP, 2019. 1117-1118.

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