Mutants and molecular dockings reveal that the primary L-thyroxine binding site in human serum albumin is not the one which can cause familial dysalbuminemic hyperthyroxinemia

Mutants and molecular dockings reveal that the primary L-thyroxine binding site in human serum albumin is not the one which can cause familial dysalbuminemic hyperthyroxinemia

Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochimica et Biophysica Acta (BBA) - General Subjects - Volume 1860, Issue 4, April 2016, Pages 648-660

Ulrich Kragh-Hansen, Lorenzo Minchiotti, Andrea Coletta, Konrad Bienk, Monica Galliano, Birgit Schiøtt, Yasunori Iwao, Yu Ishima, Masaki Otagiri,