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The vitamin is then transferred to TC2, which serves as the circulating plasma transporter, hereditary defects in the production of TC2 and its receptor may produce functional deficiencies in B 12 and infantile megaloblastic anemia, and abnormal B 12 related biochemistry, even in some cases with normal blood B 12 levels
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doi: 10.1007/s10654-014-9930-3 30 SchmidtMSchmidtSAJAdelborgKSundbollJLaugesenKEhrensteinVet al
10.1021/bi010518v Biochemistry 6 BohrerA.-S.TakahashiH
SGLT2 inhibitors have varying eGFR thresholds depending on the specific agent and indication
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