%0 Case Reports
%T Unraveling Phenotypic Variability in Action Myoclonus with Renal Failure with SCARB2 Mutation in Siblings.
%A Nair LJ
%A Vijayaraghavan A
%J Mov Disord Clin Pract
%V 11
%N 8
%D 2024 Aug 13
%M 38741477
%F 4.514
%R 10.1002/mdc3.14067