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The study, “Maternofetal and neonatal copper requirements revealed by enterocyte-specific deletion of the Menkes disease protein,” was published in the American Journal of Physiology-Gastrointestinal and Liver Physiology. Co-authors were Yanfang Wang, Sha Zhu and Gary Weisman, researchers in the MU Department of Biochemistry; Joseph Prohaska from University of Minnesota Medical School; and Jonathan Gitlin from the Marine Biological Laboratory in Woods Hole, Mass. The research was funded by a grant from the National Institutes of Health.
University of Missouri-Columbia
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University of Missouri-Columbia. "Menkes Disease: Discovery Helps Explain How Children Develop This Rare, Fatal Disease." Medical News Today. MediLexicon, Intl., 3 May. 2013. Web.
16 Apr. 2014. <http://www.medicalnewstoday.com/releases/259911>
University of Missouri-Columbia. (2013, May 3). "Menkes Disease: Discovery Helps Explain How Children Develop This Rare, Fatal Disease." Medical News Today. Retrieved from
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