Creatine transporter defect diagnosed by proton NMR spectroscopy in males with intellectual disability.

MLA

Mencarelli, Maria Antonietta, et al. “Creatine Transporter Defect Diagnosed by Proton NMR Spectroscopy in Males with Intellectual Disability.” American Journal of Medical Genetics. Part A, vol. 155A, no. 10, Oct. 2011, pp. 2446–52. EBSCOhost, https://doi.org/10.1002/ajmg.a.34208.

APA

Mencarelli, M. A., Tassini, M., Pollazzon, M., Vivi, A., Calderisi, M., Falco, M., Fichera, M., Monti, L., Buoni, S., Mari, F., Engelke, U., Wevers, R. A., Hayek, J., & Renieri, A. (2011). Creatine transporter defect diagnosed by proton NMR spectroscopy in males with intellectual disability. American Journal of Medical Genetics. Part A, 155A(10), 2446–2452. https://doi.org/10.1002/ajmg.a.34208

Chicago

Mencarelli, Maria Antonietta, Maria Tassini, Marzia Pollazzon, Antonio Vivi, Marco Calderisi, Michele Falco, Marco Fichera, et al. 2011. “Creatine Transporter Defect Diagnosed by Proton NMR Spectroscopy in Males with Intellectual Disability.” American Journal of Medical Genetics. Part A 155A (10): 2446–52. doi:10.1002/ajmg.a.34208.