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PubMed, Choi, Se Joon, et al
Patients with genetic slow-metabolizer phenotypes, liver disease, or chronic illness may warrant baseline and periodic testing
Common impurities include truncated sequences (particularly des-Gly1 and des-Val15 variants), deamidation products at Asp residues, and residual TFA from synthesis
doi: 10.1089/thy.2005.15.841 127
2016;11(11):e0163716
O n the one hand, no one nowadays questions the need to draw u p educational policies, or the right to do so
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