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Dive into the research topics of 'De novo heterozygous missense and loss-of-function variants in CDC42BPB are associated with a neurodevelopmental phenotype'. Together they form a unique fingerprint.- Sort by
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Ilana Chilton, Volkan Okur, Giuseppina Vitiello, Angelo Selicorni, Milena Mariani, Alice Goldenberg, Thomas Husson, Dominique Campion, Klaske D Lichtenbelt, Koen van Gassen, Michelle Steinraths, Jennifer Rice, Elizabeth R Roeder, Rebecca O Littlejohn, Myriam Srour, Guillaume Sebire, Andrea Accogli, Delphine Héron, Solveig Heide, Caroline Nava
Research output: Contribution to journal › Article › Academic › peer-review