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	1.	Eighteen-year follow-up of a patient with partial hypoxanthine phosphoribosyltransferase deficiency and a new mutation. [electronic resource] by Gregoric, Alojz Rabelink, Gwenda M Kokalj Vokac, Nadja Varda, Natasa Marcun Zagradisnik, Boris Producer: 20051110 In: Pediatric nephrology (Berlin, Germany) vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Novel PRKCG/SCA14 mutation in a Dutch spinocerebellar ataxia family: expanding the phenotype. [electronic resource] by Vlak, Monique H M Sinke, Richard J Rabelink, Gwenda M Kremer, Berry P H van de Warrenburg, Bart P C Producer: 20061215 In: Movement disorders : official journal of the Movement Disorder Society vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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