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Distribution of fragile X mental retardation 1 CGG repeat and flanking haplotypes in a large Chinese population
Fragile X syndrome is mainly caused by a CGG repeat expansion within the 5′ UTR of the fragile X mental retardation 1 (FMR1) gene. Previous analyses of the FMR1 CGG repeat patterns and flanking haplotypes in Caucasians and African Americans have identified several factors that may influence repeat i...
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| Publicat a: | Mol Genet Genomic Med |
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| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BlackWell Publishing Ltd
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4444158/ https://ncbi.nlm.nih.gov/pubmed/26029703 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.128 |
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