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Description
Curr Neurovasc Res (2021) 18(1):13449
Bodybuilding.com Signature Triple Carnitine
PMID 11734549
This is an attractive strategy for 3540% of Rett syndrome patients who have nonsense mutations in MECP2 that result in premature stop codons, which inhibit normal full-length protein expression (Neul et al
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