https://www.selleckchem.com/pr....oducts/Vorinostat-sa
Results The genetic analysis revealed the presence of pathogenic heterozygous c.314del (p.Pro105Leufs*7) frameshift variant in the PKP2 gene. Cascade screening of family members allowed us to identify 12 mutation carriers and to intervene on subjects at risk, many of whom were athletes. Conclusions Molecular autopsy can establish cardiogenetic diagnosis and allow appropriate preventative measures in high-risk relatives.Background Mesenchymal stromal cells (MSCs) are an attractive cell type for cell therapy given their immunomodu
Like
Comment
Share
