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...
Main Authors: | , , , , , , |
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Format: | Online |
Language: | English |
Published: |
BlackWell Publishing Ltd
2015
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Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444158/ |