Allosteric mechanism for site-specific ubiquitination of FANCD2

por Chaugule, Viduth K., Arkinson, Connor, Rennie, Martin L., Kämäräinen, Outi, Toth, Rachel, Walden, Helen
Publicado 2019

EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH)

por Porto, Graça, Brissot, Pierre, Swinkels, Dorine W, Zoller, Heinz, Kamarainen, Outi, Patton, Simon, Alonso, Isabel, Morris, Michael, Keeney, Steve
Publicado 2016