Mutations in the MPV17 gene are responsible for rapidly progressive liver failure in infancy

MPV17 is a mitochondrial inner membrane protein of unknown function recently recognized as responsible for a mitochondrial DNA depletion syndrome. The aim of this study is to delineate the specific clinical, pathological, biochemical, and molecular features associated with mitochondrial DNA depletio...

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Veröffentlicht in:Hepatology (Baltimore, Md.) Md.), 2007-10, Vol.46 (4), p.1218-1227
Hauptverfasser: Wong, Lee‐Jun C., Brunetti‐Pierri, Nicola, Zhang, Qing, Yazigi, Nada, Bove, Kevin E., Dahms, Beverly B., Puchowicz, Michelle A., Gonzalez‐Gomez, Ignacio, Schmitt, Eric S., Truong, Cavatina K., Hoppel, Charles L., Chou, Ping‐Chieh, Wang, Jing, Baldwin, Erin E., Adams, Darius, Leslie, Nancy, Boles, Richard G., Kerr, Douglas S., Craigen, William J.
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Sprache:eng
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