ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism.
Brain
; 139(Pt 1): e3, 2016 Jan.
Article
in En
| MEDLINE
| ID: mdl-26297558
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Ornithine
/
Spastic Paraplegia, Hereditary
/
Aldehyde Dehydrogenase
/
Mutation
Limits:
Female
/
Humans
/
Male
Language:
En
Journal:
Brain
Year:
2016
Document type:
Article
Affiliation country:
Italia
Country of publication:
Reino Unido