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Further phenotypical delineation of DLG3-related neurodevelopmental disorders

2025-03-10 | Preprint
DOI: 10.21203/rs.3.rs-5998122/v1
Contributors: Marlène Malbos; Thierry Gautier; Amelle Shillington; Estelle Colin; Xavier Le Guillou Horn; Oana Caluseriu; Bertrand Isidor; Benjamin Cogné; Cyril Mignot; Boris Keren et al.
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Speech and language deficits are central to SETBP1 haploinsufficiency disorder

European Journal of Human Genetics
2021-04-27 | Journal article
DOI: 10.1038/s41431-021-00894-x
Part of ISSN: 1018-4813
Part of ISSN: 1476-5438
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estelle colin
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