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Diurnal variation in autonomic regulation among patients with genotyped Rett syndrome
BACKGROUND: Rett syndrome is a severe neurological disorder with a range of disabling autonomic and respiratory symptoms and resulting predominantly from variants in the methyl-CpG binding protein 2 gene on the long arm of the X-chromosome. As basic research begins to suggest potential treatments, s...
Tallennettuna:
| Julkaisussa: | J Med Genet |
|---|---|
| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7891682/ https://ncbi.nlm.nih.gov/pubmed/32156713 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmedgenet-2019-106601 |
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