Mutation in DHP receptor Ó1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis.

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Title:	Mutation in DHP receptor Ó1 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.; Wintzen, A.R.; Deutekom, J.C.T. van
Publication year:	1995
Source:	Journal of Medical Genetics, vol. 32, (1995), pp. 44-47
ISSN:	0022-2593
DOI:	https://doi.org/10.1136/jmg.32.1.44
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/189301
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Subject:	Neuromuscular and neurometabolic disorders Neuromusculaire en neurometabole aandoeningen
Organization:	Neurology
Journal title:	Journal of Medical Genetics
Volume:	vol. 32
Page start:	p. 44
Page end:	p. 47