Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleA homozygous loss-of-function mutation in PDE2A associated to early-onset hereditary chorea.AuthorsSalpietro, Vincenzo; Perez‐Dueñas, Belen; Nakashima, Kosuke; San Antonio‐Arce, Victoria; Manole, Andreea; Efthymiou, Stephanie; Vandrovcova, Jana; Bettencourt, Conceicao; Mencacci, Niccolò E.; Klein, Christine; Kelly, Michy P.; Davies, Ceri H.; Kimura, Haruhide; Macaya, Alfons; Houlden, Henry; Perez-Dueñas, Belen; San Antonio-Arce, VictoriaPublicationMovement Disorders, 2018, Vol 33, Issue 3, p482ISSN0885-3185Publication typejournal articleDOI10.1002/mds.27286