APA (7th ed.) Citation

L, C., MF, Z., HW, D., M, L., LL, F., QB, Z., . . . JY, Y. A Novel Pathogenic Splicing Mutation of OFD1 is Responsible for a Boy with Joubert Syndrome Exhibiting Orofaciodigital Spectrum Anomalies, Polydactyly and Retinitis Pigmentosa. Dove Medical Press.

Chicago Style (17th ed.) Citation

L, Chen, et al. A Novel Pathogenic Splicing Mutation of OFD1 Is Responsible for a Boy with Joubert Syndrome Exhibiting Orofaciodigital Spectrum Anomalies, Polydactyly and Retinitis Pigmentosa. Dove Medical Press.

MLA (9th ed.) Citation

L, Chen, et al. A Novel Pathogenic Splicing Mutation of OFD1 Is Responsible for a Boy with Joubert Syndrome Exhibiting Orofaciodigital Spectrum Anomalies, Polydactyly and Retinitis Pigmentosa. Dove Medical Press.