Repeat-mediated genetic and epigenetic changes at the FMR1 locus in the Fragile X-related disorders.

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作者： Karen,Usdin ^[1] ; Bruce E,Hayward ^[1] ; Daman,Kumari ^[1] ; Rachel A,Lokanga ^[1] ; Nicholas,Sciascia ^[1] ; Xiao-Nan,Zhao ^[1]

作者单位： Section on Gene Structure and Disease, Laboratory of Cell and Molecular Biology, National Institute of Diabetes, Digestive and Kidney Diseases, National Institutes of Health, Bethesda MD, USA. ^[1]

关键词 FX-associated primary ovarian insufficiency (FXPOI)FX-associated tremor/ataxia syndrome (FXTAS)Fragile X syndrome (FXS)Fragile X-related disorders repeat expansion disease

DOI 10.3389/fgene.2014.00226

PMID 25101111

发布时间 2022-04-09

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Frontiers in genetics

2014年5卷

226页

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Repeat-mediated genetic and epigenetic changes at the FMR1 locus in the Fragile X-related disorders.

Frontiers in genetics

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Frontiers in genetics

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Repeat-mediated genetic and epigenetic changes at the FMR1 locus in the Fragile X-related disorders.

Frontiers in genetics

相似文献

Frontiers in genetics

相关期刊

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