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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-00J-F43

Author(s)

Vieira, JP

Lopes, F

Silva-Fernandes, A

Sousa, MV

Moura, S

Sousa, S

Costa, BM

Barbosa, M

Ylstra, B

Temudo, T

Lourenço, T

Maciel, P

Document Type

Article

Year published

2015

Published

in International Journal of Developmental Neuroscience, ISSN: 0736-5748

Volume: 46, Pages: 82-87

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Google Scholar^®

Publication Identifiers

DOI: 10.1016/j.ijdevneu.2015.07.010

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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