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About this Biochemistry, Genetics and Molecular Biology article

Mutations in human lipoyltransferase geneLIPT1cause a Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase by Yohan Soreze,Audrey Boutron,Florence Habarou... is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.

It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.

Author
Yohan Soreze,Audrey Boutron,Florence Habarou...
Publisher
BioMed Central; Springer (Biomed Central Ltd.); [London]: BioMed Central, 2006-; Springer Science and Business Media LLC; Society for Mining, Metallurgy and Exploration Inc. (ISSN 1750-1172)
Published
2013
Field
Biochemistry, Genetics and Molecular Biology (Life Sciences)

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