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Quanticon™ Human MGST1(Microsomal Glutathione S Transferase 1) ELISA Kit https://picx.zhimg.com/v2-6aede94924bebbd26aaaf9f823d47f09_1440w.jpg Life Stage_Teens Flavor:Strawberry watermelon Migraine Monogenic familial hemiplegic migraine (FHM) type 2 is a primary genetic astrocytopathy caused by loss-of-function mutations in the ATP1A2 gene encoding the α2 subunit of Na + /K + ATPase (the NKA) expressed solely in astrocytes 327
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