Valdez, Clarissa

Progranulin-mediated deficiency of cathepsin D results in FTD and NCL-like phenotypes in neurons derived from FTD patients

Human Molecular Genetics | September 22, 2017 | Volume: 26 | Issue: 24 | Pages: 4861-4872

10.1093/hmg/ddx364 | PMID 29036611