Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutation
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| Format: | Online |
| Language: | English |
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Oxford University Press
2011
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212709/ |
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pubmed-3212709 |
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pubmed-32127092011-11-10 Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutation Yu-Wai-Man, Patrick Chinnery, Patrick F. Letters to the Editor Oxford University Press 2011-11 2011-06-06 /pmc/articles/PMC3212709/ /pubmed/26281626 http://dx.doi.org/10.1093/brain/awr102 Text en © The Author(s) 2011. Published by Oxford University Press on behalf of Brain. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
| repository_type |
Open Access Journal |
| institution_category |
Foreign Institution |
| institution |
US National Center for Biotechnology Information |
| building |
NCBI PubMed |
| collection |
Online Access |
| language |
English |
| format |
Online |
| author |
Yu-Wai-Man, Patrick Chinnery, Patrick F. |
| spellingShingle |
Yu-Wai-Man, Patrick Chinnery, Patrick F. Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutation |
| author_facet |
Yu-Wai-Man, Patrick Chinnery, Patrick F. |
| author_sort |
Yu-Wai-Man, Patrick |
| title |
Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutation |
| title_short |
Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutation |
| title_full |
Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutation |
| title_fullStr |
Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutation |
| title_full_unstemmed |
Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutation |
| title_sort |
reply: spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to opa1 mutation |
| description |
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| publisher |
Oxford University Press |
| publishDate |
2011 |
| url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212709/ |
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1611486599662534656 |