Santos, M., Temudo, T., Kay, T., Carrilho, I., Medeira, A., Cabral, H., . . . Maciel, P. (2009). 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, Mónica, et al. Mutations in the MECP2 Gene Are Not a Major Cause of Rett Syndrome-like or Related Neurodevelopmental Phenotype in Male Patients. 2009.
MLA (8th ed.) CitationSantos, Mónica, et al. Mutations in the MECP2 Gene Are Not a Major Cause of Rett Syndrome-like or Related Neurodevelopmental Phenotype in Male Patients. 2009.
Warning: These citations may not always be 100% accurate.