Santos, M., Temudo, T., Kay, T., Carrilho, I., Medeira, A., Cabral, H., . . . Maciel, P. (2016). Mutations in the MECP2 Gene Are Not a Major Cause of Rett Syndrome-Like or Related Neurodevelopmental Phenotype in Male Patients.
Chicago Style (17th ed.) CitationSantos, M., et al. Mutations in the MECP2 Gene Are Not a Major Cause of Rett Syndrome-Like or Related Neurodevelopmental Phenotype in Male Patients. 2016.
MLA (8th ed.) CitationSantos, M., et al. Mutations in the MECP2 Gene Are Not a Major Cause of Rett Syndrome-Like or Related Neurodevelopmental Phenotype in Male Patients. 2016.
Warning: These citations may not always be 100% accurate.