Cita APA

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. Nat Commun.

Chicago Style Citation

Lee, Yu-Ri, et al. "Mutations in FAM50A Suggest That Armfield XLID Syndrome Is a Spliceosomopathy." Nat Commun 2020.

Cita MLA

Lee, Yu-Ri, et al. "Mutations in FAM50A Suggest That Armfield XLID Syndrome Is a Spliceosomopathy." Nat Commun 2020.