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A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing.

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Title: A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing.
Authors: Cao, Ye1,2,3 (AUTHOR), Tokita, Mari J.1 (AUTHOR), Chen, Edward S.1 (AUTHOR), Ghosh, Rajarshi1,2 (AUTHOR), Chen, Tiansheng2 (AUTHOR), Feng, Yanming2 (AUTHOR), Gorman, Elizabeth2 (AUTHOR), Gibellini, Federica2 (AUTHOR), Ward, Patricia A.1,2 (AUTHOR), Braxton, Alicia2 (AUTHOR), Wang, Xia1,2 (AUTHOR), Meng, Linyan1,2 (AUTHOR), Xiao, Rui1,2 (AUTHOR), Bi, Weimin1,2 (AUTHOR), Xia, Fan1,2 (AUTHOR), Eng, Christine M.1,2 (AUTHOR), Yang, Yaping1,2 (AUTHOR), Gambin, Tomasz1,4,5 (AUTHOR), Shaw, Chad1,6 (AUTHOR), Liu, Pengfei1,2 (AUTHOR) pengfeil@bcm.edu
Source: Genome Medicine. 7/26/2019, Vol. 11 Issue 1, pN.PAG-N.PAG. 1p.
Database: Academic Search Ultimate
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  Data: A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing.
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