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FAN1 protects against repeat expansions in a Fragile X mouse model.
The Fragile X-related disorders (FXDs) are members of a large group of human neurological or neurodevelopmental conditions known as the Repeat Expansion Diseases. The mutation responsible for all of these diseases is an expansion in the size of a disease-specific tandem repeat tract. However, the un...
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發表在: | DNA Repair (Amst) |
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Main Authors: | , |
格式: | Artigo |
語言: | Inglês |
出版: |
2018
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主題: | |
在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6119480/ https://ncbi.nlm.nih.gov/pubmed/29990673 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.dnarep.2018.07.001 |
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