“Myo-cardiomyopathy” is commonly associated with the A8344G “MERRF” mutation-Reference-Cited by-全球学者库

“Myo-cardiomyopathy” is commonly associated with the A8344G “MERRF” mutation

Published:2015-01-06 Issue:3 Volume:262 Page:701-710
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Catteruccia Michela,Sauchelli Donato,Della Marca Giacomo,Primiano Guido,Cuccagna Cristina,Bernardo Daniela,Leo Milena,Camporeale Antonella,Sanna Tommaso,Cianfoni Alessandro,Servidei Serenella

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-014-7632-0.pdf

Reference34 articles.

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3. DiMauro S, Servidei S, Zeviani M et al (1987) Cytochrome oxidase deficiency in Leigh syndrome. Ann Neurol 22(4):498–506

4. Zeviani M, Gellera C, Antozzi C et al (1991) Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR). Lancet 338(8760):143–147

5. Silvestri G, Servidei S, Rana M et al (1996) A Novel Mitochondrial DNA point mutation in the tRNA(Ile) gene is associated with progressive external ophthalmoplegia. Biochem Biophys Res Commun 20(2):221–225

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