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3. AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia

4. Architecture of the ESCPE-1 membrane coat

8. Regulation of angiogenesis by endocytic trafficking mediated by cytoplasmic dynein 1 light intermediate chain 1

10. Intrathecal AAV9/AP4M1 gene therapy for hereditary spastic paraplegia 50 shows safety and efficacy in preclinical studies

13. The Reelin Receptor ApoER2 is a Cargo for the Adaptor Protein Complex AP-4: Implications for Hereditary Spastic Paraplegia

14. Biallelic BORCS8 variants cause an infantile-onset neurodegenerative disorder with altered lysosome dynamics

19. How HIV-1 Nef hijacks the AP-2 clathrin adaptor to downregulate CD4.

45. PI4P and BLOC-1 remodel endosomal membranes into tubules

46. Autophagy-associated immune dysregulation and hyperplasia in a patient with compound heterozygous mutations in ATG9A

50. Autophagy-associated immune dysregulation and hyperplasia in a patient with compound heterozygous mutations in ATG9A.

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