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De novo mutations in SCN1A are associated with classic Rett syndrome: a case report
BACKGROUND: Rett syndrome (RTT) is a neurodevelopmental disorder. In more than 95% of females with classic RTT a pathogenic mutation in MECP2 has been identified. This leaves a small fraction of classic cases with other genetic causes. So far, there has not been reported any other gene that may acco...
Tallennettuna:
| Julkaisussa: | BMC Med Genet |
|---|---|
| Päätekijät: | , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2018
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6180591/ https://ncbi.nlm.nih.gov/pubmed/30305042 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-018-0700-z |
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