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1 ensaios clínicos encontrados.
Griscelli syndrome type 2: A rare case report of pediatric immunodeficiency and neurological implications.
Griscelli Syndrome Type 2 Revealed by Macrophage Activation Syndrome: Two Cases From the Same Family.
Assessment of Potential Side Effects Related To RAB27A Gene Therapy in Stem Cells.
Case Report: Late-onset primary hemophagocytic lymphohistiocytosis leading to the diagnosis of Griscelli syndrome type 2 in a young woman with phenotypically inapparent partial albinism.
Effect of genetic mutations on outcomes of stem cell transplantation in children with hemophagocytic lymphohistiocytosis.