A homozygous <i>loss‐of‐function</i> mutation in <i>PDE2A</i> associated to early‐onset hereditary chorea
Vincenzo Salpietro(University College London), Henry Houlden(Queen Mary University of London), Ceri H. Davies, Christine Klein(University of Lübeck), Stéphanie Efthymiou(Queen Mary University of London), Michy P. Kelly(University of Maryland, Baltimore), Belén Pérez‐Dueñas(Vall d'Hebron Hospital Universitari), Alfons Macaya(Universitat Autònoma de Barcelona), Conceição Bettencourt(National Hospital for Neurology and Neurosurgery), Jana Vandrovcová(Texas Tech University), Andreea Manole(National Hospital for Neurology and Neurosurgery), Haruhide Kimura(Takeda (Japan)), Kosuke Nakashima(Takeda (Japan)), Niccolò E. Mencacci(Northwestern University), Victoria San Antonio‐Arce(Hospital Sant Joan de Déu Barcelona)
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