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Full spectrum genetics
被引：7
作者：
不详
机构：
关键词：
D O I：
10.1038/ng.1057
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ;
090102 ;
摘要：
Every instance of a variant in the human genome causing or correlated with a trait deserves to be databased and analyzed. As a consequence of rapidly evolving technology and strategies, more of the mutational spectrum of human disease is now accessible to research. Advised by our referees' progressively higher standards, we continue to select the most informative and useful results.
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