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In total, 14 genomic regions have been identified as related to the disease, such as genes involved in IFN‐γ production, NKG2D‐mediated cytotoxicity (ULBP3/6, MICA, and IL2), T cell activation and proliferation (CTLA‐4, IL2, IL21, IL2RA, SOCS1, IKZF4/Eos, GARP/LRRC32, SH2B3(LNK)/ATXN2, IL23A, PTPN22, CD28, ICOS, and IL13), HLAs (HLA‐DRB1, C6orf10, BTNL2, HLA‐DRA, HLA‐DQA1, HLA‐DQA2, and HLA‐DQB2), as well as hair follicle‐related genes (STX17, PRDX5, ACOXL/BCL2L11, ERBB3, and CCHCR1) [149, 150, 151, 152, 153]

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“L-carnitine and Acetyl-L Carnitine: A Possibility for Treating Alterations Induced by Obesity in the Central Nervous System.” Neurochem Res