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New insights of altered lipid profile in Fragile X Syndrome

BACKGROUND: Fragile X Syndrome (FXS) is the main genetic cause of autism and intellectual deficiency resulting the absence of the Fragile X Mental Retardation Protein (FMRP). Clinical picture is characterized by cognitive impairment associated with a broad spectrum of psychiatric comorbidities inclu...

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Detalles Bibliográficos
Autores principales:	Çaku, Artuela, Seidah, Nabil G., Lortie, Audrey, Gagné, Nancy, Perron, Patrice, Dubé, Jean, Corbin, Francois
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2017
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363930/ https://www.ncbi.nlm.nih.gov/pubmed/28334053 http://dx.doi.org/10.1371/journal.pone.0174301

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