Chapter 30 Mitochondrial disorders-Reference-Cited by-同舟云学术

Chapter 30 Mitochondrial disorders

Published:2004 Issue: Volume: Page:304-312
ISSN:1567-424X
Container-title:Advances in Clinical Neurophysiology, Proceedings of the 27th International Congress of Clinical Neurophysiology, AAEM 50th Anniversary and 57th Annual Meeting of the ACNS Joint Meeting
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Author:

Zeviani Massimo

Publisher

Elsevier

Reference45 articles.

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2. Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA;Andreu;N. Engl. J. Med.,1999

3. Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA;Andrews;Nat. Genet.,1999

4. The mitochondrial generation of hydrogen peroxide. General properties and effect of hyperbaric oxygen;Boveris;Biochem. J.,1973

5. Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage;Brown;Am. J. Hum. Genet.,1997

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4. A1555G homoplasmic mutation from A1555G heteroplasmic mother with Pendred syndrome;International Journal of Pediatric Otorhinolaryngology;2014-11

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