Načítá se...
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...
Uloženo v:
| Vydáno v: | Intractable Rare Dis Res |
|---|---|
| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
International Research and Cooperation Association for Bio & Socio-Sciences Advancement
2016
|
| Témata: | |
| On-line přístup: | 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 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|