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Rett syndrome: think outside the (skull) box
Rett syndrome (RTT) is a severe X-linked neurodevelopmental disorder characterized by neurodevelopmental regression between 6 and 18 months of life and associated with multi-system comorbidities. Caused mainly by pathogenic variants in the MECP2 (methyl CpG binding protein 2) gene, it is the second...
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| Опубликовано в: : | Fac Rev |
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| Главные авторы: | , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Faculty Opinions Ltd
2021
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8265562/ https://ncbi.nlm.nih.gov/pubmed/34308425 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12703/r/10-59 |
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