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Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis.
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 EVolume:
32
Language:
english
Journal:
Journal of Medical Genetics
DOI:
10.1136/jmg.32.1.44
Date:
January, 1995
File:
PDF, 622 KB
english, 1995