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Rett Syndrome with and Without Detected Mecp2 Mutations: An Attempt to Redefine Phenotypes

AuthID
P-002-Y4P

Author(s)

Temudo, T

Santos, M

Ramos, E

Dias, K

Vieira, JP

Moreira, A

Calado, E

Carrilho, I

Oliveira, G

Levy, A

Barbot, C

[+4]·

Borges, L

Gomes, R

Mira, G

Pereira, SA

Santos, M

Epplen, JT

Tipo de Documento

Article

Year published

2011

Publicado

in BRAIN & DEVELOPMENT, ISSN: 0387-7604

Volume: 33, Número: 1, Páginas: 69-76 (8)

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Publication Identifiers

DOI: 10.1016/j.braindev.2010.01.004

Handle: https://hdl.handle.net/1822/19077

Pubmed: 20116947

SCOPUS: 2-s2.0-78650306582

Wos: WOS:000286910700011

Source Identifiers

ISSN: 0387-7604

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All authors

Name Order	Nome	Name Order	Nome	Name Order	Nome
1	Temudo, T;	2	Santos, M;	3	Ramos, E ;
4	Dias, K;	5	Vieira, JP;	6	Moreira, A;
7	Calado, E;	8	Carrilho, I;	9	Oliveira, G ;
10	Levy, A;	11	Barbot, C ;	12	Fonseca, M;
13	Cabral, A;	14	Cabral, P;	15	Monteiro, J;
16	Borges, L;	17	Gomes, R;	18	Mira, G;
19	Pereira, SA;	20	Santos, M;	21	Fernandes, A ;
22	Epplen, JT;	23	Sequeiros, J ;	24	Maciel, P ;

Rett Syndrome with and Without Detected Mecp2 Mutations: An Attempt to Redefine Phenotypes

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Rett Syndrome with and Without Detected Mecp2 Mutations: An Attempt to Redefine Phenotypes

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