Human Mutation is a peer-reviewed journal that offers publication of original Research Articles, Methods, Mutation Updates, Reviews, Database Articles, Rapid Communications, and Letters on broad aspects of mutation research in humans. Reports of novel DNA variations and their phenotypic consequences, reports of SNPs demonstrated as valuable for genomic analysis, descriptions of new molecular detection methods, and novel approaches to clinical diagnosis are welcomed. Novel reports of gene organization at the genomic level, reported in the context of mutation investigation, may be considered. The journal provides a unique forum for the exchange of ideas, methods, and applications of interest to molecular, human, and medical geneticists in academic, industrial, and clinical research settings worldwide.
　　《人类突变》是一本同行评议的期刊，提供原始研究文章、方法、突变更新、评论、数据库文章、快速通讯和有关人类突变研究广泛方面的信件。新的DNA变异及其表型结果的报道，SNPs对基因组分析有价值的报道，新的分子检测方法的描述，以及新的临床诊断方法受到欢迎。新的基因组织在基因组水平的报告，报告的背景下，突变研究，可以考虑。该杂志为全世界学术、工业和临床研究领域的分子、人类和医学遗传学家提供了一个独特的论坛，交流他们感兴趣的想法、方法和应用。