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This suggests that S
Rare mutations in the SLC22A5 gene can cause a genetic condition called primary carnitine deficiency, which is usually discovered in infancy because it affects brain function, muscle function, and blood glucose levels
2014 Jun 6;269:143-51 Authors: Karalija A, Novikova LN, Kingham PJ, Wiberg M, Novikov LN Abstract Traumatic spinal cord injury induces a long-standing inflammatory response in the spinal cord tissue, leading to a progressive apoptotic death of spinal cord neurons and glial cells
A deficiency can lead to fatigue and weakness
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