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Scand J Rheumatol 41(2):103109 Bekris LM, Shephard C, Peterson M, Hoehna J, Van Yserloo B, Rutledge E, Farin F, Kavanagh TJ, Lernmark A (2005) Glutathione-s-transferase M1 and T1 polymorphisms and associations with type 1 diabetes age-at-onset

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You might be surprised how many systems in your body rely on methylation to run smoothly

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This also implicates that the macrothrombocytopenia phenotype caused by GATA1 deficiency is complex and can be the result of many genes that show aberrant GATA1-drive expression, but part of the overall phenotype and especially the -granule defect could be due to NBEAL2 loss