Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndromeSandra Ammann(University of Freiburg), Stephan Ehl(University Medical Center Freiburg)BloodJanuary 7, 201610.1182/blood-2015-09-671636Cited by 177SaveCiteExport RISWatch citationsRelated PapersPatients with T<sup>+/low</sup> NK<sup>+</sup> IL‐2 receptor γ chain deficiency have differentially‐impaired cytokine signaling resulting in severe combined immunodeficiency|European Journal of Immunology|2014|34