Commentary: The mutations and clinical variability in maternally inherited diabetes and deafness: an analysis of 161 patients
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2023-06-01
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| Series: | Frontiers in Endocrinology |
| Subjects: | |
| Online Access: | https://www.frontiersin.org/articles/10.3389/fendo.2023.1205862/full |
| _version_ | 1797809775041314816 |
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| author | Ivo P. van de Peppel Ivo P. van de Peppel Serwet Demirdas Behiye Özcan |
| author_facet | Ivo P. van de Peppel Ivo P. van de Peppel Serwet Demirdas Behiye Özcan |
| author_sort | Ivo P. van de Peppel |
| collection | DOAJ |
| first_indexed | 2024-03-13T06:57:52Z |
| format | Article |
| id | doaj.art-4e000804aa8c4eea8990986f9f37ec82 |
| institution | Directory Open Access Journal |
| issn | 1664-2392 |
| language | English |
| last_indexed | 2024-03-13T06:57:52Z |
| publishDate | 2023-06-01 |
| publisher | Frontiers Media S.A. |
| record_format | Article |
| series | Frontiers in Endocrinology |
| spelling | doaj.art-4e000804aa8c4eea8990986f9f37ec822023-06-07T04:58:04ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922023-06-011410.3389/fendo.2023.12058621205862Commentary: The mutations and clinical variability in maternally inherited diabetes and deafness: an analysis of 161 patientsIvo P. van de Peppel0Ivo P. van de Peppel1Serwet Demirdas2Behiye Özcan3Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, NetherlandsDepartment of Clinical Genetics, Leiden University Medical Centre, Leiden, NetherlandsDepartment of Clinical Genetics, Erasmus Medical Centre, Rotterdam, NetherlandsDepartment of Internal Medicine, Erasmus Medical Centre, Rotterdam, Netherlandshttps://www.frontiersin.org/articles/10.3389/fendo.2023.1205862/fullMIDDheteroplasmymitochondrial diseasediabetes mellitusm.3243A>Gclinical genetics |
| spellingShingle | Ivo P. van de Peppel Ivo P. van de Peppel Serwet Demirdas Behiye Özcan Commentary: The mutations and clinical variability in maternally inherited diabetes and deafness: an analysis of 161 patients Frontiers in Endocrinology MIDD heteroplasmy mitochondrial disease diabetes mellitus m.3243A>G clinical genetics |
| 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 | MIDD heteroplasmy mitochondrial disease diabetes mellitus m.3243A>G clinical genetics |
| url | https://www.frontiersin.org/articles/10.3389/fendo.2023.1205862/full |
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