%0 Dataset
%T Realization of a Standard of Care for Rare Diseases Using Patient-Engaged Phenotyping [Methods Study], United States, 2018-2020
%A Holm, Ingrid A.
%D 2026-03-11
%R 10.3886/ICPSR39716.v1
%I Inter-university Consortium for Political and Social Research [distributor]