Associated Papers
Heterozygote MTHFR A1298C mutation in a case of autosomal recessive bestrophinopathy with branch retinal vein occlusion.
Hemmati S et al.
Ophthalmic Genetics, 2022
Association analyses suggest multiple interaction effects of the methylenetetrahydrofolate reductase polymorphisms on timing of menarche and natural menopause in white women.
Liu P et al.
Menopause (new York, N.y.), 0
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