- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISBN
-
9783540643425
3540643427
- Dimensions
-
24 cm
- Extent
-
412 S.
- Language
-
Englisch
- Notes
-
Ill., graph. Darst.
Literaturangaben
- Keyword
-
Altern
Mitochondriale DNS
Mutation
Krebs
Mitochondriale DNS
Mutation
Krankheit
Mitochondriale DNS
Mutation
Mitochondriopathie
Molekularbiologie
- Event
-
Veröffentlichung
- (where)
-
Berlin, Heidelberg, New York, Barcelona, Budapest, Hong Kong, London, Milan, Paris, Santa Clara, Singapore, Tokyo, Georgetown, TX
- (who)
-
Springer, Landes Bioscience
- (when)
-
1998
- Contributor
- Table of contents
- Rights
-
Bei diesem Objekt liegt nur das Inhaltsverzeichnis digital vor. Der Zugriff darauf ist unbeschränkt möglich.
- Last update
-
11.03.2025, 12:34 PM CET
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Object type
- Aufsatzsammlung
Associated
- Singh, Keshav K.
- Springer, Landes Bioscience
Time of origin
- 1998
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Mitochondrial mutations can alter neuromuscular transmission in congenital myasthenic syndrome and mitochondrial disease
Mutations of the Mitochondrial DNA: The Contribution of DNA Techniques to the Diagnosis of Mitochondrial Encephalomyopathies
Mitochondrial DNA mutations and respiratory chain dysfunction in idiopathic and connective tissue disease-related lung fibrosis
Natural radioactivity and human mitochondrial DNA mutations in Kerala (India)
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Development and characterization of a novel mouse model carrying mitochondrial DNA mutations
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The source and fate of mitochondrial DNA mutations using high-sensitivity next-generation sequencing technologies
The low abundance of clonally expanded mitochondrial DNA point mutations in aged substantia nigra neurons
Generating mammalian mitochondrial disease models with mitochondrial DNA mutations
Mutations in mitochondrial DNA causing tubulointerstitial kidney disease
Mutations in mitochondrial DNA causing tubulointerstitial kidney disease
Mitochondrial mutations can alter neuromuscular transmission in congenital myasthenic syndrome and mitochondrial disease
Mutations of the Mitochondrial DNA: The Contribution of DNA Techniques to the Diagnosis of Mitochondrial Encephalomyopathies
Mitochondrial DNA mutations and respiratory chain dysfunction in idiopathic and connective tissue disease-related lung fibrosis
Natural radioactivity and human mitochondrial DNA mutations in Kerala (India)
Natural radioactivity and human mitochondrial DNA mutations in Kerala (India)
Development and characterization of a novel mouse model carrying mitochondrial DNA mutations
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