Clinical phenotypes of a juvenile sibling pair carrying the fragile X premutation

Individuals with alleles containing 55–200 CGG repeats in the fragile X mental retardation (FMR1) gene are premutation carriers. The premutation allele has been shown to lead to a number of types of clinical involvement, including shyness, anxiety, social deficits, attention deficit hyperactivity di...

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Bibliographic Details
Main Authors: Basuta, Kirin, Narcisa, Vivien, Chavez, Alyssa, Kumar, Madhur, Gane, Louise, Hagerman, Randi, Tassone, Flora
Format: Artigo
Language:Inglês
Published: 2011
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Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC3568664/
https://ncbi.nlm.nih.gov/pubmed/21344625
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.33446
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