Lee, Y., Khan, K., Armfield-Uhas, K., Srikanth, S., Thompson, N. A., Pardo, M., . . . Schwartz, C. E. (2020). Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathy. Nature Portfolio.
Chicago Style (17th ed.) CitationLee, Yu-Ri, et al. Mutations in FAM50A Suggest That Armfield XLID Syndrome Is a Spliceosomopathy. Nature Portfolio, 2020.
MLA (8th ed.) CitationLee, Yu-Ri, et al. Mutations in FAM50A Suggest That Armfield XLID Syndrome Is a Spliceosomopathy. Nature Portfolio, 2020.
Warning: These citations may not always be 100% accurate.