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	1.	CLN6, which is associated with a lysosomal storage disease, is an endoplasmic reticulum protein. [electronic resource] by Mole, Sara E Michaux, Gregoire Codlin, Sandra Wheeler, Ruth B Sharp, Julie D Cutler, Daniel F Producer: 20041004 In: Experimental cell research vol. 298 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	The gene mutated in variant late-infantile neuronal ceroid lipofuscinosis (CLN6) and in nclf mutant mice encodes a novel predicted transmembrane protein. [electronic resource] by Wheeler, Ruth B Sharp, Julie D Schultz, Roger A Joslin, John M Williams, Ruth E Mole, Sara E Producer: 20020226 In: American journal of human genetics vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Spectrum of CLN6 mutations in variant late infantile neuronal ceroid lipofuscinosis. [electronic resource] by Sharp, Julie D Wheeler, Ruth B Parker, Keith A Gardiner, R Mark Williams, Ruth E Mole, Sara E Producer: 20030811 In: Human mutation vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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