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The neurobiology of the Prader-Willi phenotype of fragile X syndrome
Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability and autism, caused by a CGG expansion to greater than 200 repeats in the promoter region of FMR1 on the bottom of the X chromosome. A subgroup of individuals with FXS experience hyperphagia, lack of satiation afte...
Salvato in:
| Pubblicato in: | Intractable Rare Dis Res |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
International Research and Cooperation Association for Bio & Socio-Sciences Advancement
2016
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5116860/ https://ncbi.nlm.nih.gov/pubmed/27904820 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2016.01082 |
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