APA (7th ed.) Citation

Møller, L. B., Mogensen, M., Weaver, D. D., & Pedersen, P. A. (2021, April). Occipital Horn Syndrome as a Result of Splice Site Mutations in ATP7A. No Activity of ATP7A Splice Variants Missing Exon 10 or Exon 15. Frontiers in Molecular Neuroscience.

Chicago Style (17th ed.) Citation

Møller, Lisbeth Birk, Mie Mogensen, David D. Weaver, and Per Amstrup Pedersen. "Occipital Horn Syndrome as a Result of Splice Site Mutations in ATP7A. No Activity of ATP7A Splice Variants Missing Exon 10 or Exon 15." Frontiers in Molecular Neuroscience Apr. 2021.

MLA (9th ed.) Citation

Møller, Lisbeth Birk, et al. "Occipital Horn Syndrome as a Result of Splice Site Mutations in ATP7A. No Activity of ATP7A Splice Variants Missing Exon 10 or Exon 15." Frontiers in Molecular Neuroscience, Apr. 2021.