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doi: 10.1007/s00395-016-0588-8 104 MurphyMPSmithRA
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Disease Treatment Primary and secondary coenzyme Q 10 deficiencies Inherited coenzyme Q 10 deficiencies are rare diseases that are clinically and genetically heterogeneous (see Deficiency)
On the contrary, increasing the expression of GPX1 will bring protective effects to the corresponding tissues and organs
Many experts agree that almost every chronic illness known to humankind can be linked in some measure to free radical-induced tissue damage
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