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SMC2, encoding a core component of the condensin complex, is mutated in Hallermann-Streiff syndrome: a condensinopathy revelationEMBO workshop : Organisation of bacterial and eukaryotic genomes by SMC complexes, Sep 2019, Vienna (Austria), Austria
Conference papers
inserm-03855668v1
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De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal developmentNature Genetics, 2017, 49 (2), pp.249-255. ⟨10.1038/ng.3765⟩
Journal articles
hal-01617529v1
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