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Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations.
Arch Neurol. 2006 Sep;63(9):1250-4. doi: 10.1001/archneur.63.9.1250.
Arch Neurol. 2006.
PMID: 16966502
Juvenile-onset Parkinsonism as a result of the first mutation in the adenosine triphosphate orientation domain of PINK1.
Leutenegger AL, Salih MA, Ibáñez P, Mukhtar MM, Lesage S, Arabi A, Lohmann E, Dürr A, Ahmed AE, Brice A.
Leutenegger AL, et al.
Arch Neurol. 2006 Sep;63(9):1257-61. doi: 10.1001/archneur.63.9.1257.
Arch Neurol. 2006.
PMID: 16966503
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