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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: http://hdl.handle.net/11858/00-001M-0000-0010-8B7D-0 Version Permalink: http://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: 2002-11
 Publication Status: Published in print
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Method: -
 Identifiers: eDoc: 24161
 Degree: -

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Title: Journal of Medical Genetics
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 39 (11) Sequence Number: - Start / End Page: 812 - 816 Identifier: -