Associated Papers
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.
Jia X et al.
Molecular Psychiatry, 2021
33483695 (PubMed )
Supplement: 41380_2020_1006_MOESM2_ESM.xlsx › S2
Predicting the functional and structural consequences of nsSNPs in human methionine synthase gene using computational tools.
Desai M et al.
Systems Biology in Reproductive Medicine, 2019
Hyperhomocysteinemia due to methionine synthase deficiency, cblG: structure of the MTR gene, genotype diversity, and recognition of a common mutation, P1173L.
Watkins D et al.
American Journal of Human Genetics, 2002
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