Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.Title<italic>CKAP2L</italic> mutation confirms the diagnosis of Filippi syndrome.AuthorsCapecchi, G.; Ferranti, S.; Guidoni, E.; Cioni, M.; Grosso, S.; Baldassarri, M.; Renieri, A.; Mencarelli, M. A.; Nürnberg, P.SubjectsGENETIC disorders; MICROCEPHALY; ELECTROENCEPHALOGRAPHYPublicationClinical Genetics, 2018, Vol 93, Issue 5, p1109ISSN0009-9163Publication typeLetter to the EditorDOI10.1111/cge.13188