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KEY POINTS Choline is required to make key molecules involved in cell signalling pathways
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
Das Ergebnis ist ein reineres Hormonprofil in experimentellen Studien
Acknowledgements The authors want to express their sincere gratitude to Prof
Jiang, X
doi: 10.3390/genes12111790 42 dos Santos LopesN.Silva SantosA.de NovaisD
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