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
12
Author(s)
Vieira, JP
·
Lopes, F
·
Sousa, MV
·
Moura, S
·
Sousa, S
·
Barbosa, M
·
Ylstra, B
·
Temudo, T
·
Lourenço, T
·
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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ISSN: 0736-5748
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