ConclusionThe prevalence of the mutation genotype and the mutation allele of PAFAH exon 9 in patients with ACI is significantly increased.

结论ACI患者血浆型PAF - AH基因9号外显子突变基因型及突变等位基因显著增高。

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Their allele frequencies at numerous genetic loci gradually become more and more different as new alleles independently arise by mutation in each population.

随着新等位基因在每个群体中独立突变产生，它们在许多遗传位点上的等位基因频率逐渐变得越来越不同。

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Haploinsufficiency --- A cause of genetic disease in which the contribution from a normal allele is insufficient to prevent disease because of a loss-of-function mutation at the other allele.

遗传病的原因之一，单倍的基因剂量不足以维持正常功能。

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