Variant Rett Syndrome in a Girl with a Pericentric X-Chromosome Inversion Leading to Epigenetic Changes and Overexpression of the Mecp2 Gene

AuthID
 P-00G-JHG
12
Author(s)
Vieira, JP
·
Lopes, F
·
Sousa, MV
·
Moura, S
·
Sousa, S
·
Barbosa, M
·
Ylstra, B
·
Temudo, T
·
Lourenco, T
·
Tipo de Documento
Article
Year published
2015
Publicado
in INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, ISSN: 0736-5748
Volume: 46, Páginas: 82-87 (6)
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Publication Identifiers
SCOPUS: 2-s2.0-84940047811
Wos: WOS:000362139500012
Source Identifiers
ISSN: 0736-5748
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