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Sun L, Deng L, Ea C-K, Xia Z-P, Chen ZJ

Four alanine mutated residues, V229A, V160A, I165A, and L401A, caused a significant decrease in GLP-1R internalisation versus WT receptor, with GLP-1R V229A and V160A causing a 40%, and I165A and L401A a 30% decrease in internalisation (Figure 2H, bottom graph)

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If your MTHFR gene mutation reduces folate metabolism, the risk of pregnancy complications rises significantly, including neural tube defects (spina bifida, cleft lip/palate), Down syndrome, preeclampsia, recurrent losses and more