Supplementary Material for: Impairment of Renal Function in Hermansky-Pudlak Syndrome

Introduction Hermansky-Pudlak syndrome (HPS) is a rare autosomal recessive disorder characterized by defective biogenesis of lysosome-related organelles. The genetic types of HPS are associated with a spectrum of multisystemic clinical manifestations. Phenotypic features of HPS type 1 (HPS-1) or HPS...

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Main Author: Yokoyama T. (4606381) (author)
Other Authors: O’Brien K.J. (19810578) (author), Franklin T.M. (19810581) (author), Zuo B.L.G. (19810584) (author), Zuo M.X.G. (19810587) (author), Merideth M.A. (19810590) (author), Introne W.J. (19810593) (author), Gochuico B.R. (19810596) (author)
Published: 2024
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