Severe respiratory complex III defect prevents liver adaptation to prolonged fasting

BACKGROUND AND AIMS: Next generation sequencing approaches have tremendously improved the diagnosis of rare genetic diseases. It may however be faced with difficult clinical interpretation of variants. Inherited enzymatic diseases provide an invaluable possibility to evaluate the function of the def...

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Detalhes bibliográficos
Publicado no:J Hepatol
Main Authors: Kremer, Laura, L 'hermitte-Stead, Caroline, Lesimple, Pierre, Gilleron, Mylène, Filaut, Sandrine, Jardel, Claude, Haack, Tobias, Strom, Tim, Meitinger, Thomas, Azzouz, Hatem, Tebib, Neji, Ogier De Baulny, Hélène, Touati, Guy, Prokisch, Holger, Lombès, Anne
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2016
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5640785/
https://ncbi.nlm.nih.gov/pubmed/27151179
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jhep.2016.04.017
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