APA Alıntı

Lessel, D., Ozel, A. B., Campbell, S. E., Saadi, A., Arlt, M. F., McSweeney, K. M., . . . Gordon, L. B. (2018). Analyses of LMNA-negative juvenile progeroid cases confirms biallelic POLR3A mutations in Wiedemann-Rautenstrauch-like syndrome and expands the phenotypic spectrum of PYCR1 mutations. Hum Genet.

Chicago Stili Alıntı

Lessel, Davor, et al. "Analyses of LMNA-negative Juvenile Progeroid Cases Confirms Biallelic POLR3A Mutations in Wiedemann-Rautenstrauch-like Syndrome and Expands the Phenotypic Spectrum of PYCR1 Mutations." Hum Genet 2018.

MLA Alıntı

Lessel, Davor, et al. "Analyses of LMNA-negative Juvenile Progeroid Cases Confirms Biallelic POLR3A Mutations in Wiedemann-Rautenstrauch-like Syndrome and Expands the Phenotypic Spectrum of PYCR1 Mutations." Hum Genet 2018.