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Description
Rossana Gmez-Campos
A founder mutation in COQ7, p.(Leu111Pro), causes pure hereditary spastic paraplegia (HSP) in the Iranian population
doi:10.1371/journal.pgen.1007361
Archived from the original on August 17, 2020
The thiol antioxidant lipoic acid and Alzheimers disease
It only made sense to further harness the legendary power of Glutamine, by adding a hefty 1000mg dose of pure Vitamin C
