Cargando…
Commentary: The mutations and clinical variability in maternally inherited diabetes and deafness: an analysis of 161 patients
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10284591/ https://www.ncbi.nlm.nih.gov/pubmed/37351107 http://dx.doi.org/10.3389/fendo.2023.1205862 |
_version_ | 1785061435550728192 |
---|---|
author | van de Peppel, Ivo P. Demirdas, Serwet Özcan, Behiye |
author_facet | van de Peppel, Ivo P. Demirdas, Serwet Özcan, Behiye |
author_sort | van de Peppel, Ivo P. |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-10284591 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102845912023-06-22 Commentary: The mutations and clinical variability in maternally inherited diabetes and deafness: an analysis of 161 patients van de Peppel, Ivo P. Demirdas, Serwet Özcan, Behiye Front Endocrinol (Lausanne) Endocrinology Frontiers Media S.A. 2023-06-07 /pmc/articles/PMC10284591/ /pubmed/37351107 http://dx.doi.org/10.3389/fendo.2023.1205862 Text en Copyright © 2023 van de Peppel, Demirdas and Özcan https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology van de Peppel, Ivo P. Demirdas, Serwet Özcan, Behiye Commentary: The mutations and clinical variability in maternally inherited diabetes and deafness: an analysis of 161 patients |
title | Commentary: The mutations and clinical variability in maternally inherited diabetes and deafness: an analysis of 161 patients |
title_full | Commentary: The mutations and clinical variability in maternally inherited diabetes and deafness: an analysis of 161 patients |
title_fullStr | Commentary: The mutations and clinical variability in maternally inherited diabetes and deafness: an analysis of 161 patients |
title_full_unstemmed | Commentary: The mutations and clinical variability in maternally inherited diabetes and deafness: an analysis of 161 patients |
title_short | Commentary: The mutations and clinical variability in maternally inherited diabetes and deafness: an analysis of 161 patients |
title_sort | commentary: the mutations and clinical variability in maternally inherited diabetes and deafness: an analysis of 161 patients |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10284591/ https://www.ncbi.nlm.nih.gov/pubmed/37351107 http://dx.doi.org/10.3389/fendo.2023.1205862 |
work_keys_str_mv | AT vandepeppelivop commentarythemutationsandclinicalvariabilityinmaternallyinheriteddiabetesanddeafnessananalysisof161patients AT demirdasserwet commentarythemutationsandclinicalvariabilityinmaternallyinheriteddiabetesanddeafnessananalysisof161patients AT ozcanbehiye commentarythemutationsandclinicalvariabilityinmaternallyinheriteddiabetesanddeafnessananalysisof161patients |