Mudd's disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes.

MLA

Yin-Hsiu Chien, et al. “Mudd’s Disease (MAT I/III Deficiency): A Survey of Data for MAT1A Homozygotes and Compound Heterozygotes.” Orphanet Journal of Rare Diseases, vol. 10, no. 1, Aug. 2015, pp. 1–21. EBSCOhost, https://doi.org/10.1186/s13023-015-0321-y.

APA

Yin-Hsiu Chien, Abdenur, J. E., Baronio, F., Bannick, A. A., Corrales, F., Couce, M., Donner, M. G., Ficicioglu, C., Freehauf, C., Frithiof, D., Gotway, G., Koichi Hirabayashi, Hofstede, F., Hoganson, G., Wuh-Liang Hwu, James, P., Sook Kim, Korman, S. H., Lachmann, R., & Levy, H. (2015). Mudd’s disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes. Orphanet Journal of Rare Diseases, 10(1), 1–21. https://doi.org/10.1186/s13023-015-0321-y

Chicago

Yin-Hsiu Chien, Jose E. Abdenur, Federico Baronio, Allison Anne Bannick, Fernando Corrales, Maria Couce, Markus G. Donner, et al. 2015. “Mudd’s Disease (MAT I/III Deficiency): A Survey of Data for MAT1A Homozygotes and Compound Heterozygotes.” Orphanet Journal of Rare Diseases 10 (1): 1–21. doi:10.1186/s13023-015-0321-y.