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

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Publication year
1995
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.
Source
Journal of Medical Genetics, 32, 1, (1995), pp. 44-47
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Publication type
Article / Letter to editor
If a DOI or any other persistent identifier is unavailable, please use the following repository identifier to link to this item: https://hdl.handle.net/2066/20690   https://hdl.handle.net/2066/20690
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