A homozygous loss-of-function mutation in PDE2A associated to early-onset hereditary chorea

Vincenzo Salpietro, Belen Perez-Dueñas, Kosuke Nakashima, Victoria San Antonio-Arce, Andreea Manole, Stephanie Efthymiou, Jana Vandrovcova, Conceicao Bettencourt, Niccolò E. Mencacci, Christine Klein, Michy P. Kelly, Ceri H. Davies, Haruhide Kimura, Alfons Macaya, Henry Houlden*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

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Medicine & Life Sciences