Partial Loss of FITM2 Function Causes Hereditary Spastic Paraplegia.
Overview & Synopsis
Open access biomedical research article published in Hum Mutat.
Indexed from repository: PubMed Central
(
pmc.ncbi.nlm.nih.gov)
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Document Information
| Document Title | Partial Loss of FITM2 Function Causes Hereditary Spastic Paraplegia. |
|---|---|
| Author / Organization | Salazar-Villacorta A, Bond LM, Kim L, Anagnostopoulou K, Scardamaglia A, Filippakopoulou E, Ververi A, Efthymiou S, Dinopoulos A, Murphy D, Kartanou C, Vrachnos DM, Loupis T, Makrythanasis P, Stefanis L, Karadima G, Koutsis G, Kaliakatsos M, Houlden H, Walther TC, Farese RV |
| Subject & Discipline | Hum Mutat |
| Categories | Medicine & Health |
| Publication Year | 2026 |
| License / Rights | Open Access / Creative Commons |
| Resource Verification | Listed PDF (Verification Pending) |
| Original Host Website |
PubMed Central
(pmc.ncbi.nlm.nih.gov)
|
| File Format | application/pdf (Portable Document Format) |
| Language | EN |
| Catalog ID | DOC-31495 |
| Original Source Link | Visit Source Page on pmc.ncbi.nlm.nih.gov » |