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Physiological regulation and social-emotional processing in female carriers of the FMR1 premutation
The FMR1 gene is associated with a wide range of clinical and cognitive phenotypes, ranging from intellectual disability and autism symptoms in fragile X syndrome (caused by the FMR1 full mutation), to a more varied, and still poorly understood range of clinical and cognitive phenotypes among carrie...
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| Vydáno v: | Physiol Behav |
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| Hlavní autoři: | , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6992413/ https://ncbi.nlm.nih.gov/pubmed/31765665 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.physbeh.2019.112746 |
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