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Diagnose Kearns–Sayre syndrome genetically and investigate the phenotype comprehensively
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5782484/ https://www.ncbi.nlm.nih.gov/pubmed/29497555 http://dx.doi.org/10.1093/omcr/omw059 |
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author | Finsterer, Josef Zarrouk-Mahjoub, Sinda |
author_facet | Finsterer, Josef Zarrouk-Mahjoub, Sinda |
author_sort | Finsterer, Josef |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-5782484 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57824842018-03-01 Diagnose Kearns–Sayre syndrome genetically and investigate the phenotype comprehensively Finsterer, Josef Zarrouk-Mahjoub, Sinda Oxf Med Case Reports Letter to the Editor Oxford University Press 2016-08-29 /pmc/articles/PMC5782484/ /pubmed/29497555 http://dx.doi.org/10.1093/omcr/omw059 Text en © The Author 2016. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Letter to the Editor Finsterer, Josef Zarrouk-Mahjoub, Sinda Diagnose Kearns–Sayre syndrome genetically and investigate the phenotype comprehensively |
title | Diagnose Kearns–Sayre syndrome genetically and investigate the
phenotype comprehensively |
title_full | Diagnose Kearns–Sayre syndrome genetically and investigate the
phenotype comprehensively |
title_fullStr | Diagnose Kearns–Sayre syndrome genetically and investigate the
phenotype comprehensively |
title_full_unstemmed | Diagnose Kearns–Sayre syndrome genetically and investigate the
phenotype comprehensively |
title_short | Diagnose Kearns–Sayre syndrome genetically and investigate the
phenotype comprehensively |
title_sort | diagnose kearns–sayre syndrome genetically and investigate the
phenotype comprehensively |
topic | Letter to the Editor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5782484/ https://www.ncbi.nlm.nih.gov/pubmed/29497555 http://dx.doi.org/10.1093/omcr/omw059 |
work_keys_str_mv | AT finstererjosef diagnosekearnssayresyndromegeneticallyandinvestigatethephenotypecomprehensively AT zarroukmahjoubsinda diagnosekearnssayresyndromegeneticallyandinvestigatethephenotypecomprehensively |