Your search returned 4 results.

Results
	1.	SCA8 repeat expansions in ataxia: a controversial association. [electronic resource] by Sobrido, M J Cholfin, J A Perlman, S Pulst, S M Geschwind, D H Producer: 20011101 In: Neurology vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	The SCA12 mutation as a rare cause of spinocerebellar ataxia. [electronic resource] by Cholfin, J A Sobrido, M J Perlman, S Pulst, S M Geschwind, D H Producer: 20011207 In: Archives of neurology vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Abnormal social behaviors in mice lacking Fgf17. [electronic resource] by Scearce-Levie, K Roberson, E D Gerstein, H Cholfin, J A Mandiyan, V S Shah, N M Rubenstein, J L R Mucke, L Producer: 20080818 In: Genes, brain, and behavior vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	COMT Val158Met genotype influences neurodegeneration within dopamine-innervated brain structures. [electronic resource] by Gennatas, E D Cholfin, J A Zhou, J Crawford, R K Sasaki, D A Karydas, A Boxer, A L Bonasera, S J Rankin, K P Gorno-Tempini, M L Rosen, H J Kramer, J H Weiner, M Miller, B L Seeley, W W Producer: 20120725 In: Neurology vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)