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M.FentkerK.LoeweA.DuerrJ.HajiM.et al (2026)

However, SNCA mutations represent a rare etiology of autosomal dominant PD (Morris et al., 2024)

P., Wen Y

Cxcl1-cxcr2 signalling mediates hypertensive retinopathy by inducing macrophage infiltration

Tell your doctor if you plan to become pregnant, are pregnant, or are breastfeeding
