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Meta-analysis reveals PTPN22 1858C/T polymorphism confers susceptibility to rheumatoid arthritis in Caucasian but not in Asian population

Theranostics 11 , 22472262 (2021)

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212 However, clinical trials aimed at inhibiting glutathione synthesis were unsuccessful, despite some strategies having provided promising results

[99] A person with cobalamin C disease, a rare autosomal, recessive, inheritance disease which results in combined methylmalonic aciduria and homocystinuria), [100] can be treated with intravenous or intramuscular hydroxocobalamin