Gene: [00.0/HOKPP2] hypokalemic periodic paralysis 2;
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COM |
Plassart-1994 demonstrated genetic heterogeneity of hypokalemic periodic paralysis. They found that the disorder in a large family of French origin was not genetically linked to Chr 1q31-q32 (hypokalemic periodic paralysis 1 due to mutation in a voltage-dependent calcium channel, see GEM:01q32/CACNA1S)." |
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REF |
HET,PAT "Plassart E &: Hum Genet, 94, 551-556, 1994 |
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KEY |
myo |
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CLA |
unknown, basic |
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LOC |
RS |
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MIM |
MIM: 600304 |
