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Findings of a 1303 Korean whole-exome sequencing study
Ethnically specific data on genetic variation are crucial for understanding human biology and for clinical interpretation of variant pathogenicity. We analyzed data obtained by deep sequencing 1303 Korean whole exomes; the data were generated by three independent whole exome sequencing projects (nam...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Exp Mol Med |
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| Κύριοι συγγραφείς: | , , , , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Nature Publishing Group
2017
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5565953/ https://ncbi.nlm.nih.gov/pubmed/28706299 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/emm.2017.142 |
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