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APA Citation
Zaha, K., Matsumoto, H., Itoh, M., Saitsu, H., Kato, K., Kato, M., Ogata, S., Murayama, K., Kishita, Y., Mizuno, Y., Kohda, M., Nishino, I., Ohtake, A., Okazaki, Y., Matsumoto, N., & Nonoyama, S. (2016). dNM1L‐related encephalopathy in infancy with Leigh syndrome‐like phenotype and suppression‐burst. Clinical genetics, 90(5), 472–474. http://access.bl.uk/ark:/81055/vdc_100038789254.0x000060