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Description
However, carriers of single copies of mutations rarely have noticeable negative effects.[ref] Primary carnitine deficiency: The SLC22A5 gene encodes the carnitine transporter known as OCTN2

Modulation of steroid receptor-mediated gene expression by vitamin B6

[DOI] [PubMed] [Google Scholar] 67.Sandrin L, Fourquet B, Hasquenoph JM, Yon S, Fournier C, Mal F, et al
The peripheral neuropathy in Fabry disease is described as a small fibre neuropathy, meaning that small, unmyelinated nerve fibres are particularly affected [82]
