Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration

BACKGROUND: Duplications of MECP2 gene in males cause a syndrome characterized by distinctive clinical features, including severe to profound mental retardation, infantile hypotonia, mild dysmorphic features, poor speech development, autistic features, seizures, progressive spasticity and recurrent...

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Detalles Bibliográficos
Autores principales: Magini, Pamela, Poscente, Monica, Ferrari, Simona, Vargiolu, Manuela, Bacchelli, Elena, Graziano, Claudio, Wischmeijer, Anita, Turchetti, Daniela, Malaspina, Elisabetta, Marchiani, Valentina, Cordelli, Duccio Maria, Franzoni, Emilio, Romeo, Giovanni, Seri, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4522089/
https://www.ncbi.nlm.nih.gov/pubmed/26236399
http://dx.doi.org/10.1186/s13039-015-0164-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4522089/
https://www.ncbi.nlm.nih.gov/pubmed/26236399
http://dx.doi.org/10.1186/s13039-015-0164-1

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