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Description
2021 Apr;24(2):198-206
Introduction Rett syndrome (RTT, OMIM 312750) is a neurodevelopmental disorder that primarily affects girls and is usually caused by mutation in the X-linked gene Methyl-CpG-binding Protein 2 ( MECP2 ) (Neul et al., 2008)
Comparing oral carnitine to other options It helps to keep perspective
You can, but results are much better when paired with exercise and a healthy diet
Citrulline supplementation can support urea cycle activity and promote the production of NO
