. Author manuscript; available in PMC: 2012 Jun 1.

Published in final edited form as: Neurosci Lett. 2011 Apr 12;496(2):125–128. doi: 10.1016/j.neulet.2011.03.098

Table 1.

Clinical features of study subjects

	Men (n=93)	Women (n=82)	p-value
Age at Exam (Mean±SD)	66.6±12.4	66.7±10.96	0.943
Age at Onset (Mean±SD)	58.98±13.4	59.7±10.6	0.713
LRRK2 G2019S carrier (%)	21.5% 20/93	23.2% 19/82	0.792
Report of family history of PD in 1st degree relative(%)	17.2% 16/93	32.9% 27/82	0.016
FH in parent	11.8% (11/93)	28.1% (23/82)	0.007
FH in parent (among *LRRK2 PD)*	25.0% (5/20)	42.1% (8/19)	0.257
FH in parent (among non-LRRK2 *PD)*	8.2% (6/73)	23.8% (15/63)	0.012
FH in siblings	5.4% (5/93)	6.1% (5/82)	0.837