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	1.	Rapid-onset dystonia-parkinsonism in a child with a novel atp1a3 gene mutation. [electronic resource] by Anselm, I A Sweadner, K J Gollamudi, S Ozelius, L J Darras, B T Producer: 20090902 In: Neurology vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	X-linked creatine transporter defect: a report on two unrelated boys with a severe clinical phenotype. [electronic resource] by Anselm, I A Anselm, I M Alkuraya, F S Salomons, G S Jakobs, C Fulton, A B Mazumdar, M Rivkin, M Frye, R Poussaint, T Young Marsden, D Producer: 20061016 In: Journal of inherited metabolic disease vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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