Lamhonwah, Anne-Marie; Barić, Ivo; Lamhonwah, Jessica; Grubić, Marina; Tein, Ingrid
Cite this document
Lamhonwah, A. M., Barić, I., Lamhonwah, J., Grubić, M. & Tein, I. (2018). Attention deficit/hyperactivity disorder as an associated feature in OCTN2 deficiency with novel deletion (p.T440-Y449). Clinical Case Reports, 6. (4), 585-591. doi: 10.1002/ccr3.1316
Lamhonwah, Anne Marie, et al. "Attention deficit/hyperactivity disorder as an associated feature in OCTN2 deficiency with novel deletion (p.T440-Y449)." Clinical Case Reports, vol. 6, no. 4, 2018, pp. 585-591. https://doi.org/10.1002/ccr3.1316
Lamhonwah, Anne Marie, Ivo Barić, Jessica Lamhonwah, Marina Grubić and Ingrid Tein. "Attention deficit/hyperactivity disorder as an associated feature in OCTN2 deficiency with novel deletion (p.T440-Y449)." Clinical Case Reports 6, no. 4 (2018): 585-591. https://doi.org/10.1002/ccr3.1316
Lamhonwah, A. M., et al. (2018) 'Attention deficit/hyperactivity disorder as an associated feature in OCTN2 deficiency with novel deletion (p.T440-Y449)', Clinical Case Reports, 6(4), pp. 585-591. doi: 10.1002/ccr3.1316
Lamhonwah AM, Barić I, Lamhonwah J, Grubić M, Tein I. Attention deficit/hyperactivity disorder as an associated feature in OCTN2 deficiency with novel deletion (p.T440-Y449). Clinical Case Reports [Internet]. 2018 February 09 [cited 2024 October 10];6(4):585-591. doi: 10.1002/ccr3.1316
A. M. Lamhonwah, I. Barić, J. Lamhonwah, M. Grubić and I. Tein, "Attention deficit/hyperactivity disorder as an associated feature in OCTN2 deficiency with novel deletion (p.T440-Y449)", Clinical Case Reports, vol. 6, no. 4, pp. 585-591, February 2018. [Online]. Available at: https://urn.nsk.hr/urn:nbn:hr:105:854412. [Accessed: 10 October 2024]