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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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| Main Authors: | , , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2011
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| Fag: | |
| Online adgang: | 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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