Identification of the causal gene by whole-exome sequencing and linkage analysis.
收藏Figshare2015-12-02 更新2026-04-29 收录
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The number of functional variants (non-synonymous/splice acceptor and donor site/insertions or deletions) is listed under various filters. Variants were filtered by presence in dbSNP, 1000 Genomes, HapMap 8 or YH (Not in dbSNP 132_1000 Genomes_HapMap_YH) and control exomes (Not in dbSNP_1kgenomes_Hapmap_YH_control). (Whole/locus): indicate NS/SS/Indel variants be observed in whole exome or in locus region by linkage analysis.
创建时间：
2015-12-02
