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HARVARD Citation
Salpietro, V. et al. (2018). A homozygous loss‐of‐function mutation in PDE2A associated to early‐onset hereditary chorea. Movement disorders. 33 (3), pp. 482-488. [Online].
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Salpietro, V. et al. (2018). A homozygous loss‐of‐function mutation in PDE2A associated to early‐onset hereditary chorea. Movement disorders. 33 (3), pp. 482-488. [Online].