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Ryder B, Inbar-Feigenberg M, Glamuzina E, et al. New insights into carnitine-acylcarnitine translocase deficiency from 23 cases: Management challenges and potential therapeutic approaches. J Inherit Metab Dis. 2021;44(4):903-915doi: 10.1002/jimd.12371.
Ryder, B., Inbar-Feigenberg, M., Glamuzina, E., Halligan, R., Vara, R., Elliot, A., Coman, D., Minto, T., Lewis, K., Schiff, M., Vijay, S., Akroyd, R., Thompson, S., MacDonald, A., Woodward, A. J. M., Gribben, J. E. L., Grunewald, S., Belaramani, K., Hall, M., van der Haak, N., Devanapalli, B., Tolun, A. A., Wilson, C., & Bhattacharya, K. (2021). New insights into carnitine-acylcarnitine translocase deficiency from 23 cases: Management challenges and potential therapeutic approaches. Journal of inherited metabolic disease, 44(4), 903-915. https://doi.org/10.1002/jimd.12371
Ryder, Bryony, et al. "New insights into carnitine-acylcarnitine translocase deficiency from 23 cases: Management challenges and potential therapeutic approaches." Journal of inherited metabolic disease vol. 44,4 (2021): 903-915. doi: https://doi.org/10.1002/jimd.12371
Ryder B, Inbar-Feigenberg M, Glamuzina E, Halligan R, Vara R, Elliot A, Coman D, Minto T, Lewis K, Schiff M, Vijay S, Akroyd R, Thompson S, MacDonald A, Woodward AJM, Gribben JEL, Grunewald S, Belaramani K, Hall M, van der Haak N, Devanapalli B, Tolun AA, Wilson C, Bhattacharya K. New insights into carnitine-acylcarnitine translocase deficiency from 23 cases: Management challenges and potential therapeutic approaches. J Inherit Metab Dis. 2021 Jul;44(4):903-915. doi: 10.1002/jimd.12371. Epub 2021 Mar 29. PMID: 33634872.
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