Exome sequencing of 18,994 ethnically diverse patients with suspected rare Mendelian disorders
Heonjong Han(Unknown), Hane Lee(Orion Corporation (United Kingdom)), SoHyun Lee, Go Hun Seo(Orion Corporation (United Kingdom)), 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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