Jurkat-Rott Karin, Lehmann-Horn Frank
Department of Applied Physiology, Ulm University, Germany.
Neurology. 2004 Mar 23;62(6):1012-5. doi: 10.1212/01.wnl.0000119392.29624.88.
An R83H point mutation in KCNE3-encoded MiRP2 has been reported to cause 2% of all cases of familial periodic paralysis. The authors found MiRP2-R83H in 3 of 321 control subjects and in 5 unaffected related individuals. Provocation of an unaffected carrier with glucose or KCl did not induce weakness. The authors propose that causality criteria for mutations require exclusion of mutations in n = ln(P)/ln(1 - p(1)) ethnically matched control chromosomes (P = acceptable error probability; p(1) = mutation prevalence in patient chromosomes).
据报道,KCNE3编码的MiRP2中的R83H点突变导致了2%的家族性周期性麻痹病例。作者在321名对照受试者中的3人以及5名未受影响的亲属个体中发现了MiRP2-R83H。用葡萄糖或氯化钾刺激未受影响的携带者并未诱发肌无力。作者提出,突变的因果关系标准要求在n = ln(P)/ln(1 - p(1))条种族匹配的对照染色体中排除突变(P = 可接受的错误概率;p(1) = 患者染色体中的突变患病率)。