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Description
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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

Fertil Steril 91(2):456488 Teede HJ, Misso ML, Costello MF, Dokras A, Laven J, Moran L et al (2018) Recommendations from the international evidence-based guideline for the assessment and management of polycystic ovary syndrome

XIV Course of Neuromodulations 33 FreoU.CarronM.InnocenteF.FolettoM.NittiD.OriC
