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Diagnose Kearns–Sayre syndrome genetically and investigate the phenotype comprehensively

Detalles Bibliográficos
Autores principales: Finsterer, Josef, Zarrouk-Mahjoub, Sinda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
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
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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
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