Exome sequencing of 18,994 ethnically diverse patients with suspected rare Mendelian disorders
Heonjong Han(Orion Corporation (United Kingdom)), Hane Lee(Seoul Medical Center), SoHyun Lee, Go Hun Seo(Ulsan College), Soyeon Yang, Kisang Kwon, Yongjun Song, Jungsul Lee(Inha University Hospital), Seong‐In Hyun(Institute for Basic Science), Won Chan Jeong, Dongwook Kim(Korea Advanced Institute of Science and Technology), Jihye Kim(Harvard University), Eugene Lee, Sohyun Jang(GeneMatrix (South Korea)), Rin Khang(Samsung (South Korea)), Joohyun Han, Seung Woo Ryu(Howard Hughes Medical Institute)
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