Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS
Hong Joo Kim(St. Jude Children's Research Hospital), Nam Chul Kim(St. Jude Children's Research Hospital), Yong‐Dong Wang(St. Jude Children's Research Hospital), Emily A. Scarborough(University of Pennsylvania), Jennifer C. Moore(St. Jude Children's Research Hospital), Zamia Diaz(University of Pennsylvania), Kyle S. MacLea(Colorado State University), Brian D. Freibaum(St. Jude Children's Research Hospital), Songqing Li(St. Jude Children's Research Hospital), Amandine Molliex(St. Jude Children's Research Hospital), Anderson Kanagaraj(St. Jude Children's Research Hospital), Robert Carter(St. Jude Children's Research Hospital), Khrista Boylan(WinnMed), Aleksandra Wojtas(Jacksonville College), Rosa Rademakers(Jacksonville College), Jack L. Pinkus(Harvard University), Steven A. Greenberg(Brigham and Women's Hospital), John Q. Trojanowski(Institute on Aging), Bryan J. Traynor(National Institute on Aging), Bradley Smith(Institute on Aging), Simon Topp(King's College London), Athina-Soragia Gkazi(King's College London), Jack W. Miller(King's College London), Christopher E. Shaw(King's College London), Michael Kottlors(University of Freiburg), Janbernd Kirschner(University of Freiburg), Alan Pestronk(Washington University in St. Louis), Leslie A. Lange(University of Pennsylvania), Alice F. Ford(University of Pennsylvania), Aaron D. Gitler(Stanford University), Michael Benatar(University of Miami), Oliver D. King(Boston Biomedical Research Institute), Virginia Kimonis(University of California, Irvine), Eric D. Ross(Colorado State University), Conrad C. Weihl(Washington University in St. Louis), James Shorter(University of Pennsylvania), J. Paul Taylor(St. Jude Children's Research Hospital)
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