Mitochondrial disease: elucidating genetic aetiology by variant discovery, validation, and integration with clinical phenotype
- Weitere Titel
-
Mitochondriale Erkrankung: Aufklärung der genetischen Ätiologie durch Identifizierung, Validierung und Integration von Varianten mit klinischen Phänotypen
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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München, Technische Universität München, Dissertation, 2021
- Schlagwort
-
Phenotype
Diseases--Causes and theories of causation
- Ereignis
-
Veröffentlichung
- (wo)
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München
- (wer)
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Universitätsbibliothek der TU München
- (wann)
-
2021
- Urheber
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Stenton, Sarah Louise
- Beteiligte Personen und Organisationen
-
Meitinger, Thomas
Freisinger, Peter
Zschocke, Johannes
Klopstock, Thomas
- URN
-
urn:nbn:de:bvb:91-diss-20210913-1610905-1-8
- Rechteinformation
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
25.03.2025, 13:44 MEZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
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Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Stenton, Sarah Louise
- Meitinger, Thomas
- Freisinger, Peter
- Zschocke, Johannes
- Klopstock, Thomas
- Universitätsbibliothek der TU München
Entstanden
- 2021
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