Mutation in DHP receptor alpha1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis

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Title:	Mutation in DHP receptor alpha1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis
Author(s):	Boerman, R.H.; Ophoff, R.A.; Links, T.P.; Eijk, R. van ; Sandkuijl, L.A.; Elbaz, A.; Vale-Santos, J.E.; Wintzen, A.R.; Deutekom, J.C.T. van; Isles, D.E.; Fontaine, B.; Padberg, G.W.; Frants, R.R.
Publication year:	1995
Source:	Journal of Medical Genetics, vol. 32, iss. 1, (1995), pp. 44-47
ISSN:	0022-2593
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/20690
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Organization:	Nijmeegs Instituut voor Missiologie (NIM)
Journal title:	Journal of Medical Genetics
Volume:	vol. 32
Issue:	iss. 1
Page start:	p. 44
Page end:	p. 47

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