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	1.	A calcium channel mutation causing hypokalemic periodic paralysis. [electronic resource] by Jurkat-Rott, K Lehmann-Horn, F Elbaz, A Heine, R Gregg, R G Hogan, K Powers, P A Lapie, P Vale-Santos, J E Weissenbach, J Producer: 19950110 In: Human molecular genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis. [electronic resource] by Boerman, R H Ophoff, R A Links, T P van Eijk, R Sandkuijl, L A Elbaz, A Vale-Santos, J E Wintzen, A R van Deutekom, J C Isles, D E Producer: 19950427 In: Journal of medical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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