The Human Mitochondrial DNA Depletion Syndrome Gene MPV17 Encodes a Non-selective Channel That Modulates Membrane Potential-Reference-Cited by-同舟云学术

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The Human Mitochondrial DNA Depletion Syndrome Gene MPV17 Encodes a Non-selective Channel That Modulates Membrane Potential

Published:2015-05 Issue:22 Volume:290 Page:13840-13861
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Antonenkov Vasily D.,Isomursu Antti,Mennerich Daniela,Vapola Miia H.,Weiher Hans,Kietzmann Thomas,Hiltunen J. Kalervo

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference66 articles.

1. MPV17-associated hepatocerebral mitochondrial DNA depletion syndrome: new patients and novel mutations;El-Hattab;Mol. Genet. Metab,2010

2. MPV17-related hepatocerebral mitochondrial DNA depletion syndrome;El-Hattab,2012

3. Mitochondrial DNA depletion syndromes: review and updates of genetic basis, manifestations, and therapeutic options;El-Hattab;Neurotherapeutics,2013

4. MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion;Spinazzola;Nat. Genet,2006

5. Clinical, biochemical and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 gene;Uusimaa;Eur. J. Hum. Genet,2014

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