Harvard Catalyst Profiles

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A PARK2 Mutation in A Consanguineous Lebanese Family Affected with Early-onset Parkinson Disease

Verlaan DJ, Fantaneanu TA, Meijer I, Rochefort D, Bedard M, Jabbour R, Rouleau GA. A PARK2 Mutation in A Consanguineous Lebanese Family Affected with Early-onset Parkinson Disease. Middle Eastern Journal of Age and Ageing. 2007; 3(4):3-6.


Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.