Spastic paraplegia in 'dominant optic atrophy plus' phenotype due to OPA1 mutation
Brain
.
2011 Nov;134(Pt 11):e195.
doi: 10.1093/brain/awr101.
Epub 2011 Jun 6.
Authors
Elena Pretegiani
,
Alessandra Rufa
,
Gian Nicola Gallus
,
Elena Cardaioli
,
Alessandro Malandrini
,
Antonio Federico
PMID:
21646330
DOI:
10.1093/brain/awr101
No abstract available
Publication types
Letter
Comment
MeSH terms
Central Nervous System Diseases / complications*
Female
GTP Phosphohydrolases / genetics*
Humans
Male
Optic Atrophy, Autosomal Dominant / complications*
Substances
GTP Phosphohydrolases
Grants and funding
G0701386/MRC_/Medical Research Council/United Kingdom