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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

Author(s)

Vieira, JP

Lopes, F

Silva Fernandes, A

Sousa, MV

Moura, S

Sousa, S

Costa, BM

Barbosa, M

Ylstra, B

Temudo, T

Lourenco, T

Maciel, P

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

DOI: 10.1016/j.ijdevneu.2015.07.010

SCOPUS: 2-s2.0-84940047811

Wos: WOS:000362139500012

Source Identifiers

ISSN: 0736-5748

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

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

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