Spectrum of combined respiratory chain defects-Reference-Cited by-同舟云学术

Spectrum of combined respiratory chain defects

Published:2015-03-17 Issue:4 Volume:38 Page:629-640
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Mayr Johannes A.,Haack Tobias B.,Freisinger Peter,Karall Daniela,Makowski Christine,Koch Johannes,Feichtinger René G.,Zimmermann Franz A.,Rolinski Boris,Ahting Uwe,Meitinger Thomas,Prokisch Holger,Sperl Wolfgang

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10545-015-9831-y

Reference127 articles.

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3. Anderson S, Bankier AT, Barrell BG et al (1981) Sequence and organization of the human mitochondrial genome. Nature 290:457–465

4. Antonicka H, Ostergaard E, Sasarman F et al (2010) Mutations in C12orf65 in patients with encephalomyopathy and a mitochondrial translation defect. Am J Hum Genet 87:115–122

5. Balreira A, Boczonadi V, Barca E et al (2014) ANO10 mutations cause ataxia and coenzyme Q10 deficiency. J Neurol 261:2192–2198

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