Clinical usefulness of comprehensive genetic screening in maturity onset diabetes of the young (MODY) : A novel ABCC8 mutation in a previously screened family
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2018 |
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| Erschienen: |
2018 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:10 |
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| Enthalten in: |
Journal of diabetes - 10(2018), 9 vom: 09. Sept., Seite 764-767 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Johnson, Stephanie R [VerfasserIn] |
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| Links: |
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| Themen: |
ABCC8 |
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| Anmerkungen: |
Date Completed 12.07.2019 Date Revised 12.07.2019 published: Print-Electronic Citation Status MEDLINE |
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| doi: |
10.1111/1753-0407.12778 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM283732563 |
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| 245 | 1 | 0 | |a Clinical usefulness of comprehensive genetic screening in maturity onset diabetes of the young (MODY) |b A novel ABCC8 mutation in a previously screened family |
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| 650 | 4 | |a hyperinsulinism | |
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| 650 | 4 | |a whole exome sequencing | |
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| 700 | 1 | |a Harris, Mark |e verfasserin |4 aut | |
| 700 | 1 | |a Brown, Matthew A |e verfasserin |4 aut | |
| 700 | 1 | |a Duncan, Emma L |e verfasserin |4 aut | |
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