APA citiranje

D’Amico, A., Fattori, F., Bellacchio, E., Catteruccia, M., Servidei, S., & Bertini, E. (2013). A new de novo missense mutation in MYH2 expands clinical and genetic findings in hereditary myosin myopathies. Pergamon Press.

Citação norma Chicago

D’Amico, A., F. Fattori, E. Bellacchio, M. Catteruccia, S. Servidei, and E. Bertini. A New De Novo Missense Mutation in MYH2 Expands Clinical and Genetic Findings in Hereditary Myosin Myopathies. Pergamon Press, 2013.

MLA citiranje

D’Amico, A., et al. A New De Novo Missense Mutation in MYH2 Expands Clinical and Genetic Findings in Hereditary Myosin Myopathies. Pergamon Press, 2013.