APA (7th ed.) Citation

Melchionda, L., Fang, M., Wang, H., Fugnanesi, V., Morbin, M., Liu, X., . . . Zeviani, M. (2013). Adult-onset Alexander disease, associated with a mutation in an alternative GFAP transcript, may be phenotypically modulated by a non-neutral HDAC6 variant. Orphanet Journal of Rare Diseases, 8(1), 1. https://doi.org/10.1186/1750-1172-8-66

Chicago Style (17th ed.) Citation

Melchionda, Laura, et al. "Adult-onset Alexander Disease, Associated with a Mutation in an Alternative GFAP Transcript, May Be Phenotypically Modulated by a Non-neutral HDAC6 Variant." Orphanet Journal of Rare Diseases 8, no. 1 (2013): 1. https://doi.org/10.1186/1750-1172-8-66.

MLA (9th ed.) Citation

Melchionda, Laura, et al. "Adult-onset Alexander Disease, Associated with a Mutation in an Alternative GFAP Transcript, May Be Phenotypically Modulated by a Non-neutral HDAC6 Variant." Orphanet Journal of Rare Diseases, vol. 8, no. 1, 2013, p. 1, https://doi.org/10.1186/1750-1172-8-66.