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Additional file 1: Table S1. of Microdeletions in 9q33.3-q34.11 in five patients with intellectual disability, microcephaly, and seizures of incomplete penetrance: is STXBP1 not the only causative gene?

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posted on 2015-09-29, 05:00 authored by Julia Ehret, Hartmut Engels, Kirsten Cremer, Jessica Becker, Johannes Zimmermann, Eva Wohlleber, Ute Grasshoff, Eva Rossier, Michael Bonin, Elisabeth Mangold, Andrea Bevot, Stefanie SchÜn, Stefanie Heilmann-Heimbach, Nicola Dennert, Michèle Mathieu-Dramard, Elodie Lacaze, Ghislaine Plessis, Alain de Broca, Guillaume Jedraszak, Benno RÜthlisberger, Peter Miny, Isabel Filges, Andreas Dufke, Joris Andrieux, Jennifer Lee, Alexander Zink
Sequencing results of GARNL3 in 192 patients with ID/DD.

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