APA

Daroszewska A., van 't Hof R. J., Rojas J. A., Layfield R., Landao-Basonga E., Rose L., Rose K. & Ralston S. H. (20111011). A point mutation in the ubiquitin-associated domain of SQSMT1 is sufficient to cause a Paget's disease-like disorder in mice. : Human molecular genetics.

Chicago

Daroszewska Anna, van 't Hof Robert J, Rojas Javier A, Layfield Robert, Landao-Basonga Euphemie, Rose Lorraine, Rose Ken and Ralston Stuart H. 20111011. A point mutation in the ubiquitin-associated domain of SQSMT1 is sufficient to cause a Paget's disease-like disorder in mice. : Human molecular genetics.

Harvard

Daroszewska A., van 't Hof R. J., Rojas J. A., Layfield R., Landao-Basonga E., Rose L., Rose K. and Ralston S. H. (20111011). A point mutation in the ubiquitin-associated domain of SQSMT1 is sufficient to cause a Paget's disease-like disorder in mice. : Human molecular genetics.

MLA

Daroszewska Anna, van 't Hof Robert J, Rojas Javier A, Layfield Robert, Landao-Basonga Euphemie, Rose Lorraine, Rose Ken and Ralston Stuart H. A point mutation in the ubiquitin-associated domain of SQSMT1 is sufficient to cause a Paget's disease-like disorder in mice. : Human molecular genetics. 20111011.