Mujtaba, G., Schultz, J. M., Imtiaz, A., Morell, R. J., Friedman, T. B., & Naz, S. (2015). A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss. J Med Genet.
Chicago Style aipamenaMujtaba, Ghulam, Julie M. Schultz, Ayesha Imtiaz, Robert J. Morell, Thomas B. Friedman, and Sadaf Naz. "A Mutation of MET, Encoding Hepatocyte Growth Factor Receptor, Is Associated With Human DFNB97 Hearing Loss." J Med Genet 2015.
MLA aipamenaMujtaba, Ghulam, et al. "A Mutation of MET, Encoding Hepatocyte Growth Factor Receptor, Is Associated With Human DFNB97 Hearing Loss." J Med Genet 2015.
Kontuz: berrikusi erreferentzia hauek erabili aurretik.