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Fragile X- associated Neuropsychiatric Disorders: A Case Report
Mutations in the Fragile X Mental Retardation 1 (FMR1) gene create a spectrum of developmental disorders in children in addition to neurodegenerative problems in older populations. Two types of mutations are recognized in the FMR1 gene. The full mutation (>200 CGG repeats) in the FMR1 gene leads...
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| Pubblicato in: | Future Neurol |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7034938/ https://ncbi.nlm.nih.gov/pubmed/32089651 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2217/fnl-2018-0040 |
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