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

AuthID
P-003-0JG

Author(s)

Vieira, JP

Silva Fernandes, A

Moura, S

Maciel, P

Tipo de Documento

Abstract

Year published

2010

Publicado

in INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, ISSN: 0736-5748

Volume: 28, Número: 8, Páginas: 683-684 (2)

Conference

18Th Biennial Meeting of the International-Society-For-Developmental-Neuroscience, Date: JUN 06-09, 2010, Location: Estoril, PORTUGAL, Patrocinadores: Int Soc Dev Neurosci

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Publication Identifiers

DOI: 10.1016/j.ijdevneu.2010.07.125

Wos: WOS:000284967600122

Source Identifiers

ISSN: 0736-5748

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

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

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