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A newly characterized AT-hook domain in MeCP2 determines clinical course of Rett syndrome and related disorders
Mutations in the X-linked MECP2 cause Rett syndrome, a devastating neurological disorder typified by a period of apparently normal development followed by loss of cognitive and psychomotor skills. Data from rare male patients suggest symptom onset and severity can be influenced by the location of th...
Tallennettuna:
| Päätekijät: | , , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2013
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3641682/ https://ncbi.nlm.nih.gov/pubmed/23452848 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cell.2013.01.038 |
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