Changing phenotypic expression in a patient with a mitochondrial encephalopathy due to 13042G>A de novo mutation—a 5 year follow up
Schinwelski, M., Kierdaszuk, B., Dulski, J., Tońska, K., Kodroń, A., Sitek, E. J., Bartnik, E., Kamińska, A., Kwieciński, H., Sławek, J.
Published in Metabolic brain disease (01.08.2015)
Published in Metabolic brain disease (01.08.2015)
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