Loading...
A novel remitting leukodystrophy associated with a variant in FBP2
Leukodystrophies are genetic disorders of cerebral white matter that almost exclusively have a progressive disease course. We became aware of three members of a family with a disorder characterized by a sudden loss of all previously acquired abilities around 1 year of age followed by almost complete...
Na minha lista:
| Udgivet i: | Brain Commun |
|---|---|
| Main Authors: | , , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Oxford University Press
2021
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8097510/ https://ncbi.nlm.nih.gov/pubmed/33977262 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/braincomms/fcab036 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|