Caricamento...
Pharmacologic rescue of axon growth defects in a human iPSC model of hereditary spastic paraplegia SPG3A
Hereditary spastic paraplegias are a large, diverse group of neurological disorders (SPG1-71) with the unifying feature of prominent lower extremity spasticity, owing to a length-dependent axonopathy of corticospinal motor neurons. The most common early-onset form of pure, autosomal dominant heredit...
Salvato in:
| Autori principali: | , , , , |
|---|---|
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2014
|
| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4189900/ https://ncbi.nlm.nih.gov/pubmed/24908668 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu280 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|