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Distribution of OCA2 *481Thr and OCA2 *615Arg, associated with hypopigmentation, in several additional populations.

机译:与色素沉着不足相关的OCA2 * 481Thr和OCA2 * 615Arg的分布在另外几个人群中。

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摘要

Two mutants, OCA2 *481Thr (c.1441G>A, p.Ala481Thr) and OCA2 *615Arg (c.1844A>G, p.His615Arg), in the OCA2 (oculocutaneous albinism type II) gene are associated with hypopigmentation in East Asians. Here, these two alleles were studied to assess the frequencies in five different populations. In addition, the allele frequency of OCA2 *615Arg was investigated in seven populations. Among a total of 24 global populations investigated, Oroqens in Heihe showed the highest frequency for OCA2 *481Thr (0.519), and among 26 populations, Han Chinese in Changsha showed the highest frequency for OCA2 *615Arg (0.673). This study confirmed that these two East Asian-specific alleles are characteristic of northern and central-southern East Asian populations.
机译:OCA2(眼白化白化病II型)基因中的两个突变体OCA2 * 481Thr(c.1441G> A,p.Ala481Thr)和OCA2 * 615Arg(c.1844A> G,p.His615Arg)与东亚人色素沉着有关。在这里,对这两个等位基因进行了研究,以评估五个不同种群中的频率。此外,在七个人群中研究了OCA2 * 615Arg的等位基因频率。在调查的全球24个人口中,黑河的Oroqens出现OCA2 * 481Thr的频率最高(0.519),而在长沙的汉族26个人口中,OCA2 * 615Arg的频率最高(0.673)。这项研究证实,这两个特定于东亚的等位基因是北亚和中南部东亚人口的特征。

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