Infantile Progressive Hepatoencephalomyopathy with Combined OXPHOS Deficiency due to Mutations in the Mitochondrial Translation Elongation Factor Gene GFM1

Por Balasubramaniam, S., Choy, Y. S., Talib, A., Norsiah, M. D., van den Heuvel, L. P., Rodenburg, R. J.
Publicado em 2011