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    Malicdan, M. C. V., Vilboux, T., Ben‐Zeev, B., Guo, J., Eliyahu, A., Pode‐Shakked, B., Dori, A., Kakani, S., Chandrasekharappa, S. C., Ferreira, C. R., Shelestovich, N., Marek‐Yagel, D., Pri‐Chen, H., Blatt, I., Niederhuber, J. E., He, L., Toro, C., Taylor, R. W., Deeken, J., Yardeni, T., Wallace, D. C., Gahl, W. A., & Anikster, Y. (2018). a novel inborn error of the coenzyme Q10 biosynthesis pathway: cerebellar ataxia and static encephalomyopathy due to COQ5 C‐methyltransferase deficiency. Human mutation, 39(1), 69–79. http://access.bl.uk/ark:/81055/vdc_100054920858.0x00002c
  
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