Cargando…
Nonsyndromic Parkinson disease in a family with autosomal dominant optic atrophy due to OPA1 mutations
| Autores principales: | , , , , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Wolters Kluwer
2017
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610041/ https://www.ncbi.nlm.nih.gov/pubmed/28955727 http://dx.doi.org/10.1212/NXG.0000000000000188 |
| _version_ | 1783265717096808448 |
|---|---|
| author | Lynch, David S. Loh, Samantha H.Y. Harley, Jasmine Noyce, Alastair J. Martins, L. Miguel Wood, Nicholas W. Houlden, Henry Plun-Favreau, Helene |
| author_facet | Lynch, David S. Loh, Samantha H.Y. Harley, Jasmine Noyce, Alastair J. Martins, L. Miguel Wood, Nicholas W. Houlden, Henry Plun-Favreau, Helene |
| author_sort | Lynch, David S. |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-5610041 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2017 |
| publisher | Wolters Kluwer |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-56100412017-09-27 Nonsyndromic Parkinson disease in a family with autosomal dominant optic atrophy due to OPA1 mutations Lynch, David S. Loh, Samantha H.Y. Harley, Jasmine Noyce, Alastair J. Martins, L. Miguel Wood, Nicholas W. Houlden, Henry Plun-Favreau, Helene Neurol Genet Clinical/Scientific Notes Wolters Kluwer 2017-09-22 /pmc/articles/PMC5610041/ /pubmed/28955727 http://dx.doi.org/10.1212/NXG.0000000000000188 Text en Copyright © 2017 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology This is an open access article distributed under the terms of the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
| spellingShingle | Clinical/Scientific Notes Lynch, David S. Loh, Samantha H.Y. Harley, Jasmine Noyce, Alastair J. Martins, L. Miguel Wood, Nicholas W. Houlden, Henry Plun-Favreau, Helene Nonsyndromic Parkinson disease in a family with autosomal dominant optic atrophy due to OPA1 mutations |
| title | Nonsyndromic Parkinson disease in a family with autosomal dominant optic atrophy due to OPA1 mutations |
| title_full | Nonsyndromic Parkinson disease in a family with autosomal dominant optic atrophy due to OPA1 mutations |
| title_fullStr | Nonsyndromic Parkinson disease in a family with autosomal dominant optic atrophy due to OPA1 mutations |
| title_full_unstemmed | Nonsyndromic Parkinson disease in a family with autosomal dominant optic atrophy due to OPA1 mutations |
| title_short | Nonsyndromic Parkinson disease in a family with autosomal dominant optic atrophy due to OPA1 mutations |
| title_sort | nonsyndromic parkinson disease in a family with autosomal dominant optic atrophy due to opa1 mutations |
| topic | Clinical/Scientific Notes |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5610041/ https://www.ncbi.nlm.nih.gov/pubmed/28955727 http://dx.doi.org/10.1212/NXG.0000000000000188 |
| work_keys_str_mv | AT lynchdavids nonsyndromicparkinsondiseaseinafamilywithautosomaldominantopticatrophyduetoopa1mutations AT lohsamanthahy nonsyndromicparkinsondiseaseinafamilywithautosomaldominantopticatrophyduetoopa1mutations AT harleyjasmine nonsyndromicparkinsondiseaseinafamilywithautosomaldominantopticatrophyduetoopa1mutations AT noycealastairj nonsyndromicparkinsondiseaseinafamilywithautosomaldominantopticatrophyduetoopa1mutations AT martinslmiguel nonsyndromicparkinsondiseaseinafamilywithautosomaldominantopticatrophyduetoopa1mutations AT woodnicholasw nonsyndromicparkinsondiseaseinafamilywithautosomaldominantopticatrophyduetoopa1mutations AT houldenhenry nonsyndromicparkinsondiseaseinafamilywithautosomaldominantopticatrophyduetoopa1mutations AT plunfavreauhelene nonsyndromicparkinsondiseaseinafamilywithautosomaldominantopticatrophyduetoopa1mutations |