Genetic Paradoxes in an Italian Family with PARK2 Multiexon Duplication

Mov Disord Clin Pract. 2017 Sep 8;4(6):889-892. doi: 10.1002/mdc3.12531. eCollection 2017 Nov-Dec.

Authors

Simona Petrucci^{1

2}, Gina Ferrazzano³, Monia Ginevrino^{1

4}, Manuela Tolve⁵, Isabella Berardelli², Alfredo Berardelli^{2

3}, Giovanni Fabbrini^{2

3}, Enza Maria Valente^{1

4}

Affiliations

¹ Neurogenetics Unit Istituto di Ricovero e Cura a Carattere Scientifico Santa Lucia Foundation Rome Italy.
² Department of Neurology and Psychiatry "Sapienza" University of Rome Rome Italy.
³ Neuromed Institute Istituto di Ricovero e Cura a Carattere Scientifico Pozzilli Italy.
⁴ Department of Molecular Medicine University of Pavia Pavia Italy.
⁵ Department of Experimental Medicine "Sapienza" University of Rome Rome Italy.

No abstract available

Keywords: Park2; Parkin; duplication; early onset Parkinson disease; phenotype.

Publication types

Case Reports

Grants and funding

260888/ERC_/European Research Council/International