DOI:
10.1055/s-00000071
Seminars in Neurology
LinksClose Window
References
Antonicka H, Ostergaard E, Sasarman F , et al.
Mutations in C12orf65 in patients with encephalomyopathy and a mitochondrial translation defect.
Am J Hum Genet 2010;
87 (1) 115-122
Search in:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.