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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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Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: Çaku, Artuela, Seidah, Nabil G., Lortie, Audrey, Gagné, Nancy, Perron, Patrice, Dubé, Jean, Corbin, Francois
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5363930/
https://ncbi.nlm.nih.gov/pubmed/28334053
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0174301
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