Mutations in the Mecp2 Gene Are Not a Major Cause of Rett Syndrome-Like or Related Neurodevelopmental Phenotype in Male Patients

AuthID
 P-003-QV4
13
Author(s)
Santos, M
·
Carrilho, I
·
Medeira, A
·
Cabral, H
·
Gomes, R
·
Lourenco, MT
·
Venancio, M
·
Tipo de Documento
Article
Year published
2009
Publicado
in JOURNAL OF CHILD NEUROLOGY, ISSN: 0883-0738
Volume: 24, Número: 1, Páginas: 49-55 (7)
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Scopus®
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Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 19168818
SCOPUS: 2-s2.0-59349100853
Wos: WOS:000262019600009
Source Identifiers
ISSN: 0883-0738
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