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OP5 – 2696: Pyruvate dehydrogenase complex deficiency: Phenotype–genotype, phenotype–neuroimaging associations and treatment outcomes
Sofou, K., Kollberg, G., Mitsis, M., Michael, E., Viggedal, G., Holme, E., Hallböök, T., Tulinius, M., Darin, N.Volume:
19
Language:
english
Journal:
European Journal of Paediatric Neurology
DOI:
10.1016/s1090-3798(15)30006-4
Date:
May, 2015
File:
PDF, 79 KB
english, 2015