A study entitled “IER3IP1-mutations cause microcephaly by selective inhibition of ER-Golgi transport”, now published in the open access journal “Cellular and Molecular Life Sciences”, provides new insights into the molecular causes of a rare and usually fatal hereditary disease called MEDS1.
Opinion | All Specialties Struggle With ‘Moral Injury’
Emily Hutto is an Associate Video Producer & Editor for MedPage Today. She is based in Manhattan. In this exclusive Instagram Live clip, Jeremy Faust,