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Nassaji M, Ghorbani R, Taheri R, Azizzadeh M, ABBASSYAN F

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It functions as a cofactor for methylmalonyl-CoA mutase in mitochondrial metabolism

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)