首页> The American journal of pathology> Oxyphil cell metaplasia in the parathyroids is characterized by somatic mitochondrial DNA mutations in NADH dehydrogenase genes and cytochrome c oxidase activity-impairing genes.

Oxyphil cell metaplasia in the parathyroids is characterized by somatic mitochondrial DNA mutations in NADH dehydrogenase genes and cytochrome c oxidase activity-impairing genes.

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第一作者： Josef,Müller-Höcker

第一单位： Institute for Pathology of the Ludwig-Maximilians-Universität München, Munich, Germany.

作者： Josef,Müller-Höcker ^[1] ; Sabine,Schäfer ^[1] ; Stefan,Krebs ^[2] ; Helmut,Blum ^[2] ; Gábor,Zsurka ^[3] ; Wolfram S,Kunz ^[3] ; Holger,Prokisch ^[4] ; Peter,Seibel ^[5] ; Andreas,Jung ^[6]

作者单位： Institute for Pathology of the Ludwig-Maximilians-Universität München, Munich, Germany. ^[1] Gene Center of the Ludwig-Maximilians-Universität München, Campus Großhadern, Munich, Germany. ^[2] Division of Neurochemistry, Department of Epileptology and Life and Brain Center, University of Bonn, Bonn, Germany. ^[3] Institute of Human Genetics, Helmholtz-Zentrum München, Neuherberg, Germany. ^[4] Molekulare Zellbiologie, Biotechnological Biomedical Center, Universität Leipzig, Leipzig, Germany. ^[5] Institute for Pathology of the Ludwig-Maximilians-Universität München, Munich, Germany; German Cancer Consortium and German Cancer Research Center, Heidelberg, Germany. Electronic address: andreas.jung@lmu.de. ^[6]