Cargando…
Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutation
| Autores principales: | , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2011
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212709/ https://www.ncbi.nlm.nih.gov/pubmed/26281626 http://dx.doi.org/10.1093/brain/awr102 |
| _version_ | 1782216012345638912 |
|---|---|
| author | Yu-Wai-Man, Patrick Chinnery, Patrick F. |
| author_facet | Yu-Wai-Man, Patrick Chinnery, Patrick F. |
| author_sort | Yu-Wai-Man, Patrick |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-3212709 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2011 |
| publisher | Oxford University Press |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-32127092011-11-10 Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutation Yu-Wai-Man, Patrick Chinnery, Patrick F. Brain 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. |
| spellingShingle | Letters to the Editor Yu-Wai-Man, Patrick Chinnery, Patrick F. Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutation |
| title | 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_short | 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 |
| topic | Letters to the Editor |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212709/ https://www.ncbi.nlm.nih.gov/pubmed/26281626 http://dx.doi.org/10.1093/brain/awr102 |
| work_keys_str_mv | AT yuwaimanpatrick replyspasticparaplegiaindominantopticatrophyplusphenotypeduetoopa1mutation AT chinnerypatrickf replyspasticparaplegiaindominantopticatrophyplusphenotypeduetoopa1mutation |