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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Main Authors: Willemsen, M.H., Rensen, J.H.M., van Schrojenstein-Lantman de Valk, H.M.J., Hamel, B.C.J., Kleefstra, T.
Formato: Artigo
Idioma:Inglês
Publicado: S. Karger AG 2012
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Paper
Acceso en liña: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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