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[1][6] More than 95% of affected individuals demonstrate a homozygous deletion/mutation involving exon 7 in SMN1 (survival motor neuron 1), resulting in the biochemical deficiency of the SMN protein, part of a complex that functions in the assembly of small nuclear ribonucleoprotein particles (snRNP)

However, contact your healthcare provider if you notice: Persistent fatigue beyond typical medication adjustment Upper right abdominal discomfort Dark urine or pale stools Yellowing of skin or eyes (jaundice) Nausea that worsens rather than improves over time These symptoms are uncommon but warrant evaluation

Int J Nutr Pharmacol Neurol Dis 11:303308

But first a quick fun fact: did you know glutamine and glutathione share a similar origin story