Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop 
mutation in the mitochondrial cytochrome c oxidase III gene

Horváth, R.; Scharfe, C.; Hoeltzenbein, M.; Do, B. H.; Schröder, C.; Warzok, R.; Vogelgesang, S.; Lochmüller, H.; Müller-Höcker, J.; Gerbitz, K. D.; Oefner, P. J.; Jaksch, M.

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Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene

Horváth, R., Scharfe, C., Hoeltzenbein, M., Do, B. H., Schröder, C., Warzok, R., et al. (2002). Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene. Journal of Medical Genetics, 39(11), 812-816.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0010-8B7D-0 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0010-8B7E-E

Genre: Journal Article

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Creators:
Horváth, R., Author
Scharfe, C., Author
Hoeltzenbein, M.¹, Author
Do, B. H., Author
Schröder, C., Author
Warzok, R., Author
Vogelgesang, S., Author
Lochmüller, H., Author
Müller-Höcker, J., Author
Gerbitz, K. D., Author
Oefner, P. J., Author
Jaksch, M., Author

Affiliations:
1Max Planck Society, ou_persistent13

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Free keywords: COXIII stop mutation; lactic acidosis; mtDNA

Abstract: No abstract.

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Language(s): eng - English

Dates: Date issued: 2002-11

Publication Status: Issued

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Identifiers: eDoc: 24161

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Title: Journal of Medical Genetics

Source Genre: Journal

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Pages: - Volume / Issue: 39 (11) Sequence Number: - Start / End Page: 812 - 816 Identifier: -