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Low Levels of HDL in Fragile X Syndrome Patients

Fragile X syndrome (FXS) is the most common form of familial mental retardation and one of the leading known causes of autism. The mutation responsible for FXS is a large expansion of the CGG repeats in the promoter region of the FMR1 gene resulting in the transcriptional silencing of the gene in th...

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Detalhes bibliográficos
Publicado no:Lipids
Main Authors: Lisik, Małgorzata Z., Gutmajster, Ewa, Sieroń, Aleksander L.
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Berlin Heidelberg 2015
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4735238/
https://ncbi.nlm.nih.gov/pubmed/26712713
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11745-015-4109-6
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