Partial Loss of FITM2 Function Causes Hereditary Spastic Paraplegia

Research paper from Europe PMC. Evidence status: source reported.

Published

2026-01-01

Source reference

PMC:PMC13691184

Jurisdiction

Not assessed

Licence

Bibliographic metadata only; article rights retained

Bond L, Filippakopoulou E, Dinopoulos A, Kartanou C, Makrythanasis P, Stefanis L, Karadima G, Koutsis G. · Hum Mutat · research-article; journal article · Found via: Genomics England

Source: https://europepmc.org/article/PMC/PMC13691184. Captured 2026-10-24.

Limitations: Discovered through a Europe PMC keyword search for Genomics England. A mention is not a verified link to an access authorisation, project, dataset or clinical outcome. Preprints may not be peer reviewed.