{Reference Type}: Case Reports
{Title}: Unraveling Phenotypic Variability in Action Myoclonus with Renal Failure with SCARB2 Mutation in Siblings.
{Author}: Nair LJ;Vijayaraghavan A;
{Journal}: Mov Disord Clin Pract
{Volume}: 11
{Issue}: 8
{Year}: 2024 Aug 13
{Factor}: 4.514
{DOI}: 10.1002/mdc3.14067