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Project

Role of rare variants in genetic predisposition to statin myopathy (NT14025)

The project objective is to determine the contribution of rare gene variants in SLCO1B1, SLCO1B3, and other known or unknown candidate genes to the mechanism of statin-induced myopathy. The presence of variants in approximately 70 patients w...

FA - Kardiovaskulární nemoci včetně kardiochirurgie

  • 2013 - 2015
  • 5 865 tis. Kč
  • 5 865 tis. Kč
  • MZ
  • 1 - 1 out of 1