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Description
C-terminal region of HBx is crucial for mitochondrial DNA damage
Similarly in PD, autosomal dominant genetic mutations such as leucine-rich repeat kinase 2 (LRRK2) and autosomal recessive mutations in the parkin genes (PRKN and PINK1) are common [4, 5]
While the latter two have been substantiated with in vitro work 133,134 , clinical efficacy has been documented for the treatment of corneal disorders with UVA-activated riboflavin, resulting in its incorporation in routine ophthalmologic procedures 135
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