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A family with two female compound heterozygous for the FMR1 premutation alleles
Premutation alleles (55-200 CGG repeats) of the fragile X mental retardation (FMR1) gene have been linked to various types of clinical involvement ranging from mood and anxiety disorders to immunological disorders and executive function deficits. Carrier females typically have a premutation allele a...
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| Huvudupphovsmän: | , , , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2013
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3996450/ https://ncbi.nlm.nih.gov/pubmed/23786467 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cge.12218 |
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