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.
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2015-12-02
