Clinical Delineation and Localization to Chromosome 9p13.3–p12 of a Unique Dominant Disorder in Four Families: Hereditary Inclusion Body Myopathy, Paget Disease of Bone, and Frontotemporal Dementia
Margaret J. Kovach(Southern Illinois University School of Medicine), Brook Waggoner(Southern Illinois University School of Medicine), Suzanne M. Leal(Rockefeller University), David A. Gelber(Springfield Clinic), Romesh Khardori(Southern Illinois University School of Medicine), Mark A. Levenstien(Rockefeller University), Christy A. Shanks(Southern Illinois University School of Medicine), Gregory Gregg(St. John's Hospital), Muhammad Al‐Lozi(Washington University in St. Louis), Timothy M. Miller(Washington University in St. Louis), Wojtek Rakowicz(Washington University in St. Louis), Glenn Lopate(Washington University in St. Louis), Juliane Florence(Washington University in St. Louis), Guila Glosser(University of Pennsylvania), Zachary Simmons(Pennsylvania State University), John C. Morris(University Memory and Aging Center), Michael P. Whyte(Washington University in St. Louis), Alan Pestronk(Washington University in St. Louis), Virginia Kimonis(Southern Illinois University School of Medicine)
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