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Erratum

机译：勘误表

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The authors regret that a mistake in Figure 4, in which clearly summarized the known desmin (DES) mutations, was made in our manuscript [1]. We searched for known DES mutations from the Leiden Open Variation Database (LOVD), Human Gene Mutation Database (HGMD), and Online Mendelian Inheritance in Man (OMIM). Unfortunately, a DES mutation located in helix 1B domain was recorded as K241fsX244 in these databases, which was originally described as K239fsX242 in a paper published by Schroder et al. [2].

机译：作者感到遗憾的是，图4中的一个错误清楚地概括了已知的结蛋白（DES）突变，这是我们的手稿[1]。我们从莱顿开放变异数据库（LOVD），人类基因突变数据库（HGMD）和人类在线孟德尔遗传（OMIM）中搜索了已知的DES突变。不幸的是，在这些数据库中，位于螺旋1B结构域的DES突变被记录为K241fsX244，最初在Schroder等人的论文中被描述为K239fsX242。 [2]。

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《Neuropathology and applied neurobiology》 |2012年第2期|共1页
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