APA (7th ed.) Citation

Khan, M., Cassidy, E., Parkin, T., Wallace, A., Carter, B., Whitehouse, W., . . . Bunn, L. (2025). My A–T pack: A qualitative study of the utility, acceptability, design, and content of a family-designed and owned information pack relevant to the lives of children and young people living with ataxia telangiectasia. Orphanet Journal of Rare Diseases, 20(1), 1. https://doi.org/10.1186/s13023-025-03919-6

Chicago Style (17th ed.) Citation

Khan, Munira, Elizabeth Cassidy, Tracey Parkin, Amanda Wallace, Bernie Carter, William Whitehouse, James Munro, Joanne Paton, and Lisa Bunn. "My A–T Pack: A Qualitative Study of the Utility, Acceptability, Design, and Content of a Family-designed and Owned Information Pack Relevant to the Lives of Children and Young People Living with Ataxia Telangiectasia." Orphanet Journal of Rare Diseases 20, no. 1 (2025): 1. https://doi.org/10.1186/s13023-025-03919-6.

MLA (9th ed.) Citation

Khan, Munira, et al. "My A–T Pack: A Qualitative Study of the Utility, Acceptability, Design, and Content of a Family-designed and Owned Information Pack Relevant to the Lives of Children and Young People Living with Ataxia Telangiectasia." Orphanet Journal of Rare Diseases, vol. 20, no. 1, 2025, p. 1, https://doi.org/10.1186/s13023-025-03919-6.