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The most frequent genetic causes of SLOCA are heterozygous GAA expansions in FGF14 (spinocerebellar atrophy type 27B) and biallelic expansions in RFC1 (cerebellar ataxia with neuropathy and vestibular areflexia (CANVAS))

Compliance Disclaimer BPC-157 & TB-500 & GHK-Cu Peptide Blend is supplied strictly for laboratory research and analytical purposes only

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In females specifically, IN delivery suppressed PI3K-AKT-mTOR signaling (FDR = 0.062)