Expanding the phenotypic and molecular spectrum of NFS1-related disorders that cause functional deficiencies in mitochondrial and cytosolic iron-sulfur cluster containing enzymes.

MLA

Yang, Jennifer H., et al. “Expanding the Phenotypic and Molecular Spectrum of NFS1-Related Disorders That Cause Functional Deficiencies in Mitochondrial and Cytosolic Iron-Sulfur Cluster Containing Enzymes.” Human Mutation, vol. 43, no. 3, Mar. 2022, pp. 305–15. EBSCOhost, https://doi.org/10.1002/humu.24330.

APA

Yang, J. H., Friederich, M. W., Ellsworth, K. A., Frederick, A., Foreman, E., Malicki, D., Dimmock, D., Lenberg, J., Prasad, C., Yu, A. C., Anthony Rupar, C., Hegele, R. A., Manickam, K., Koboldt, D. C., Crist, E., Choi, S. S., Farhan, S. M. K., Harvey, H., Sattar, S., … Wigby, K. (2022). Expanding the phenotypic and molecular spectrum of NFS1-related disorders that cause functional deficiencies in mitochondrial and cytosolic iron-sulfur cluster containing enzymes. Human Mutation, 43(3), 305–315. https://doi.org/10.1002/humu.24330

Chicago

Yang, Jennifer H, Marisa W Friederich, Katarzyna A Ellsworth, Aliya Frederick, Emily Foreman, Denise Malicki, David Dimmock, et al. 2022. “Expanding the Phenotypic and Molecular Spectrum of NFS1-Related Disorders That Cause Functional Deficiencies in Mitochondrial and Cytosolic Iron-Sulfur Cluster Containing Enzymes.” Human Mutation 43 (3): 305–15. doi:10.1002/humu.24330.