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Multisystem mitochondrial disease caused by a rare m.10038G>A mitochondrial tRNA(Gly) (MT-TG) variant
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164964/ https://www.ncbi.nlm.nih.gov/pubmed/32337339 http://dx.doi.org/10.1212/NXG.0000000000000413 |
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author | Poole, Olivia V. Horga, Alejandro Hardy, Steven A. Bugiardini, Enrico Woodward, Cathy E. Hargreaves, Iain P. Merve, Ashirwad Quinlivan, Rosaline Taylor, Robert W. Hanna, Michael G. Pitceathly, Robert D.S. |
author_facet | Poole, Olivia V. Horga, Alejandro Hardy, Steven A. Bugiardini, Enrico Woodward, Cathy E. Hargreaves, Iain P. Merve, Ashirwad Quinlivan, Rosaline Taylor, Robert W. Hanna, Michael G. Pitceathly, Robert D.S. |
author_sort | Poole, Olivia V. |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-7164964 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer |
record_format | MEDLINE/PubMed |
spelling | pubmed-71649642020-04-24 Multisystem mitochondrial disease caused by a rare m.10038G>A mitochondrial tRNA(Gly) (MT-TG) variant Poole, Olivia V. Horga, Alejandro Hardy, Steven A. Bugiardini, Enrico Woodward, Cathy E. Hargreaves, Iain P. Merve, Ashirwad Quinlivan, Rosaline Taylor, Robert W. Hanna, Michael G. Pitceathly, Robert D.S. Neurol Genet Clinical/Scientific Notes Wolters Kluwer 2020-03-18 /pmc/articles/PMC7164964/ /pubmed/32337339 http://dx.doi.org/10.1212/NXG.0000000000000413 Text en Copyright © 2020 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 Poole, Olivia V. Horga, Alejandro Hardy, Steven A. Bugiardini, Enrico Woodward, Cathy E. Hargreaves, Iain P. Merve, Ashirwad Quinlivan, Rosaline Taylor, Robert W. Hanna, Michael G. Pitceathly, Robert D.S. Multisystem mitochondrial disease caused by a rare m.10038G>A mitochondrial tRNA(Gly) (MT-TG) variant |
title | Multisystem mitochondrial disease caused by a rare m.10038G>A mitochondrial tRNA(Gly) (MT-TG) variant |
title_full | Multisystem mitochondrial disease caused by a rare m.10038G>A mitochondrial tRNA(Gly) (MT-TG) variant |
title_fullStr | Multisystem mitochondrial disease caused by a rare m.10038G>A mitochondrial tRNA(Gly) (MT-TG) variant |
title_full_unstemmed | Multisystem mitochondrial disease caused by a rare m.10038G>A mitochondrial tRNA(Gly) (MT-TG) variant |
title_short | Multisystem mitochondrial disease caused by a rare m.10038G>A mitochondrial tRNA(Gly) (MT-TG) variant |
title_sort | multisystem mitochondrial disease caused by a rare m.10038g>a mitochondrial trna(gly) (mt-tg) variant |
topic | Clinical/Scientific Notes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164964/ https://www.ncbi.nlm.nih.gov/pubmed/32337339 http://dx.doi.org/10.1212/NXG.0000000000000413 |
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