Common Variant Associations with Fragile X Syndrome

Fragile X syndrome is rare but a prominent cause of intellectual disability. It is usually caused by a de novo mutation that occurs on multiple haplotypes and thus would not be expected to be detectible using genome-wide association (GWA). We conducted GWA in 89 male FXS cases and 266 male controls,...

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Gepubliceerd in:Mol Psychiatry
Hoofdauteurs: Crowley, James J, Szatkiewicz, Jin, Kähler, Anna K, Giusti-Rodriguez, Paola, Ancalade, NaEshia, Booker, Jessica K, Carr MT, Jennifer L, Crawford, Greg E, Losh, Molly, Stockmeier, Craig A, Taylor, Annette K, Piven, Joseph, Sullivan, Patrick F
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2018
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Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6457435/
https://ncbi.nlm.nih.gov/pubmed/30531935
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41380-018-0290-3
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