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The mechanism is analogous to combining an MAOI with a serotonergic peptide like P21, a nootropic peptide derived from Cerebrolysin that crosses the blood-brain barrier and enhances hippocampal neurogenesis

The condition is inherited in an X-linked recessive manner and is associated with mutations in the AR gene Spinal muscular atrophy (SMA) an autosomal recessive disease caused by a genetic defect in the SMN1 gene which codes for a protein necessary for survival of motor neurons Footnotes Publisher's Disclaimer: This is a PDF file of an unedited manuscript that has been accepted for publication

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