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

Internet

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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