Open AccessSpastic paraplegia in 'dominant optic atrophy plus' phenotype due to OPA1 mutation
Author(s) -
Elena Pretegiani,
Alessandra Rufa,
Gian Nicola Gallus,
Elena Cardaioli,
Alessandro Malandrini,
Antonio Federico
Publication year - 2011
Publication title -
brain
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.142
H-Index - 336
eISSN - 1460-2156
pISSN - 0006-8950
DOI - 10.1093/brain/awr101
Subject(s) - hereditary spastic paraplegia , atrophy , mutation , paraplegia , phenotype , spastic , medicine , pathology , neuroscience , genetics , physical medicine and rehabilitation , biology , gene , spinal cord , cerebral palsy
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