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Editorial
2016

Polyhydramnios and cerebellar atrophy: a prenatal presentation of mitochondrial encephalomyopathy caused by mutations in the FBXL4 gene

van Rij, M. C., Jansen, F. A. R., Hellebrekers, D. M. E. I., Onkenhout, W., Smeets, B., Hendrickx, A. T., Gottschalk, R. W. H., Steggerda, S. J., Peeters-Scholte, C. M. P. C. D., Haak, M. C. & Hilhorst-Hofstee, Y., Apr 2016, In : Clinical Case Reports. 4, 4, p. 425-428

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Open Access