Larsen, M., Rost, S., El Hajj, N., Ferbert, A., Deschauer, M., Walter, M. C., . . . Müller, C. R. (2015). Diagnostic approach for FSHD revisited: SMCHD1 mutations cause FSHD2 and act as modifiers of disease severity in FSHD1. Eur J Hum Genet.
Chicago-tyylinen lähdeviittausLarsen, Mirjam, et al. "Diagnostic Approach for FSHD Revisited: SMCHD1 Mutations Cause FSHD2 and Act As Modifiers of Disease Severity in FSHD1." Eur J Hum Genet 2015.
MLA-viiteLarsen, Mirjam, et al. "Diagnostic Approach for FSHD Revisited: SMCHD1 Mutations Cause FSHD2 and Act As Modifiers of Disease Severity in FSHD1." Eur J Hum Genet 2015.
Varoitus: Nämä viitteet eivät aina ole täysin luotettavia.