International evaluation of unrecognizably uglifying human faces in late and severe secondary hyperparathyroidism in chronic kidney disease. Sagliker syndrome. A unique catastrophic entity, cytogenetic studies for chromosomal abnormalities, calcium-sensing receptor gene and GNAS1 mutations. Striking and promising missense mutations on the GNAS1 gene exons 1, 4, 10, 4
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Combined QM/MM and Monte Carlo study for redox leveling in Mn and Fe superoxide dismutase
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Published in Journal of biological inorganic chemistry (01.03.2018)
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