Spastic paraplegia in 'dominant optic atrophy plus' phenotype due to OPA1 mutation.
about
Differential diagnosis of Mendelian and mitochondrial disorders in patients with suspected multiple sclerosisDominant optic atrophy.The optic nerve: a "mito-window" on mitochondrial neurodegenerationClinical variability in hereditary optic neuropathies: Two novel mutations in two patients with dominant optic atrophy and Wolfram syndrome.Autosomal dominant hereditary optic neuropathy (ADOA): a review of the genetics and clinical manifestations of ADOA and ADOA+.Disturbed mitochondrial dynamics and neurodegenerative disorders.'Behr syndrome' with OPA1 compound heterozygote mutations.Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutation.
P2860
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P2860
Spastic paraplegia in 'dominant optic atrophy plus' phenotype due to OPA1 mutation.
description
2011 nî lūn-bûn
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2011年の論文
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name
Spastic paraplegia in 'dominant optic atrophy plus' phenotype due to OPA1 mutation.
@en
Spastic paraplegia in 'dominant optic atrophy plus' phenotype due to OPA1 mutation.
@nl
type
label
Spastic paraplegia in 'dominant optic atrophy plus' phenotype due to OPA1 mutation.
@en
Spastic paraplegia in 'dominant optic atrophy plus' phenotype due to OPA1 mutation.
@nl
prefLabel
Spastic paraplegia in 'dominant optic atrophy plus' phenotype due to OPA1 mutation.
@en
Spastic paraplegia in 'dominant optic atrophy plus' phenotype due to OPA1 mutation.
@nl
P2093
P356
P1433
P1476
Spastic paraplegia in 'dominant optic atrophy plus' phenotype due to OPA1 mutation.
@en
P2093
Alessandra Rufa
Alessandro Malandrini
Antonio Federico
Elena Cardaioli
Elena Pretegiani
Gian Nicola Gallus
P356
10.1093/BRAIN/AWR101
P407
P577
2011-06-06T00:00:00Z