Whole-exome sequencing identification of non-synonymous SNP variants of 10 CHI patients.
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*Mutation reported in Human Genome Mutation Database( HGMD). PolyPhen/SIFT: (−) benign or tolerated; (+) possibly damaging/DAMAGING Low confidence; (++) probably damaging/DAMAGING. In bold known causative genes.
创建时间：
2013-07-15
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