Mutation in DHP receptor Ó1 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.
Wintzen, A.R.
Deutekom, J.C.T. van
Source
Journal of Medical Genetics, 32, (1995), pp. 44-47
ISSN
DOI
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/189301   https://hdl.handle.net/2066/189301
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