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	1.	LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8. [electronic resource] by Nichols, W C Elsaesser, V E Pankratz, N Pauciulo, M W Marek, D K Halter, C A Rudolph, A Shults, C W Foroud, T Producer: 20080303 In: Neurology vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset. [electronic resource] by Nichols, W C Pankratz, N Marek, D K Pauciulo, M W Elsaesser, V E Halter, C A Rudolph, A Wojcieszek, J Pfeiffer, R F Foroud, T Producer: 20090220 In: Neurology vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Variation in GIGYF2 is not associated with Parkinson disease. [electronic resource] by Nichols, W C Kissell, D K Pankratz, N Pauciulo, M W Elsaesser, V E Clark, K A Halter, C A Rudolph, A Wojcieszek, J Pfeiffer, R F Foroud, T Producer: 20090714 In: Neurology vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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