CRISPR/Cas9-Mediated in vivo Genetic Correction in a Mouse Model of Hemophilia A https://t.co/7IhiJiFJDw
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RT @FrontCellDevBio: New Research: CRISPR/Cas9-Mediated in vivo Genetic Correction in a Mouse Model of Hemophilia A: Hemophilia A (HA), a c…
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RT @FrontCellDevBio: New Research: CRISPR/Cas9-Mediated in vivo Genetic Correction in a Mouse Model of Hemophilia A: Hemophilia A (HA), a c…
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New Research: CRISPR/Cas9-Mediated in vivo Genetic Correction in a Mouse Model of Hemophilia A: Hemophilia A (HA), a common bleeding disorder caused by a deficiency of coagulation factor VIII (FVIII), has long been considered an attractive… https://t.co/TR