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Automated screening for Fragile X premutation carriers based on linguistic and cognitive computational phenotypes
Millions of people globally are at high risk for neurodegenerative disorders, infertility or having children with a disability as a result of the Fragile X (FX) premutation, a genetic abnormality in FMR1 that is underdiagnosed. Despite the high prevalence of the FX premutation and its effect on publ...
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| Publicado no: | Sci Rep |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group UK
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5454004/ https://ncbi.nlm.nih.gov/pubmed/28572606 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-02682-4 |
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