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Differential increases of specific FMR1 mRNA isoforms in premutation carriers
BACKGROUND: Over 40% of males and ~16% of female carriers of a premutation FMR1 allele (55-200 CGG repeats) will develop Fragile X associated Tremor/Ataxia Syndrome (FXTAS), an adult onset neurodegenerative disorder while, about 20% of female carriers will develop Fragile X-associated Primary Ovaria...
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| I publikationen: | J Med Genet |
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| Huvudupphovsmän: | , , , , , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
2014
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4394606/ https://ncbi.nlm.nih.gov/pubmed/25358671 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmedgenet-2014-102593 |
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