VMD2
收藏国家生物信息中心2025-10-11 更新2025-03-15 收录
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http://www.uni-wuerzburg.de/humangenetics/vmd2
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资源简介：
Direct sequencing showed that these abnormal profiles were due to monoallelic transitions and transversions. We also found three polymorphic sequence changes that have been reported previously and annotated to an online database
直接测序（Direct Sequencing）结果显示，上述异常谱型源于单等位基因的碱基转换（transition）与颠换（transversion）。本研究同时发现三例既往已报道的多态性序列变异，且这些变异已被在线数据库完成注释。
提供机构：
Paris Descartes University
创建时间：
2018-02-09
