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Adult Phenotypes in Angelman- and Rett-Like Syndromes
BACKGROUND: Angelman- and Rett-like syndromes share a range of clinical characteristics, including intellectual disability (ID) with or without regression, epilepsy, infantile encephalopathy, postnatal microcephaly, features of autism spectrum disorder, and variable other neurological symptoms. The...
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| Huvudupphovsmän: | , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
S. Karger AG
2012
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3366698/ https://ncbi.nlm.nih.gov/pubmed/22670143 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000335661 |
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