Rett syndrome with and without detected MECP2 mutations: An attempt to redefine phenotypes

Title	Rett syndrome with and without detected MECP2 mutations: An attempt to redefine phenotypes
Publication Type	Journal Article
Year of Publication	2011
Authors	Temudo, T, Santos, M, Ramos, E, Dias, K, Vieira, JP, Moreira, A, Calado, E, Carrilho, I, Oliveira, G, Levy, A, Barbot, C, Fonseca, M, Cabral, A, Cabral, P, Monteiro, J, Borges, L, Gomes, R, Mira, G, Aires Pereira, S, Santos, M, Fernandes, A, Epplen, JT, Sequeiros, J, MacIel, P
Journal	Brain and Development
Volume	33
Issue	1
Pagination	69 - 76
Date Published	2011///
URL	http://www.scopus.com/inward/record.url?eid=2-s2.0-78650306582&partnerID=40&md5=dbee11e58af80969218350cb4b562c2e

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