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This complicates genotype-to-phenotype correlations in these individuals as it is difficult to infer which mutation is primarily responsible for deficient enzyme function and the clinical phenotype
(31786822) To avoid dosing errors, simply use the regimen your pharmacy is familiar with
MTSL caused peak broadening near the labeled residues, allowing us to identify which region of the FOXO4 FHD was close to the p53 TAD
PubMed Khorram O, et al
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