https://www.selleckchem.com/pr....oducts/cyclo-rgdyk.h
Choroideremia (CHM) is a rare monogenic, X-linked recessive inherited chorioretinal dystrophy caused by loss of function variants in the CHM gene. We successfully generated a novel human induced pluripotent stem cell (hiPSC) line from a CHM patient with CHM variant using the Sendai-virus based approach. These cells will provide a disease model for further studies on the disease pathogenesis and potential interventions. Hemodynamically normal pediatric trauma patients with solid organ injury receive nonoperative management. Prior res
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