APA (7th ed.) Citation

Feldt-Rasmussen, U., Dobrovolny, R., Nazarenko, I., Ballegaard, M., Hasholt, L., Rasmussen, Å. K., . . . Desnick, R. J. (2011). Diagnostic dilemma: A young woman with Fabry disease symptoms, no family history, and a “sequencing cryptic” α-galactosidase a large deletion. Molecular Genetics & Metabolism, 104(3), 314. https://doi.org/10.1016/j.ymgme.2011.05.008

Chicago Style (17th ed.) Citation

Feldt-Rasmussen, Ulla, et al. "Diagnostic Dilemma: A Young Woman with Fabry Disease Symptoms, No Family History, and a “sequencing Cryptic” α-galactosidase a Large Deletion." Molecular Genetics & Metabolism 104, no. 3 (2011): 314. https://doi.org/10.1016/j.ymgme.2011.05.008.

MLA (9th ed.) Citation

Feldt-Rasmussen, Ulla, et al. "Diagnostic Dilemma: A Young Woman with Fabry Disease Symptoms, No Family History, and a “sequencing Cryptic” α-galactosidase a Large Deletion." Molecular Genetics & Metabolism, vol. 104, no. 3, 2011, p. 314, https://doi.org/10.1016/j.ymgme.2011.05.008.