Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis.

Author:

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 E

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference34 articles.

1. Periodic paralysis;Schipperheyn, J.J.; Wintzen, A.R.; Buruma, O.J.S.;Vol; ofClinical Neurology,1992

2. Paramyotonia congenita or hyperkalemic periodic paralysis? Clinical and electrophysiological features of each entity in one family;SM, De Silva; RW, Kuncl; JW, Griffin; DR, Cornblath; S, Chavous-Tic;Muscle Nerve,1990

3. Hyperkalemic periodic paralysis and the adult sodium channel alphasubunit gene;Fontaine, B.; Khurana, T.S.; Hoffman, E.P.;Science,1990

4. Paramyotonia congenita and hyperkalemic periodic paralysis are linked to the adult muscle sodium channel gene;Ebers, G.C.; George, A.L.; Barchi, R.L.;Ann Neurol,1991

5. Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17;Koch, M.C.; Ricker, K.; Otto, M.;Hum Genet,1991

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