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Molecular and Clinical Aspects of Angelman Syndrome
The Angelman syndrome is caused by disruption of the UBE3A gene and is clinically delineated by the combination of severe mental disability, seizures, absent speech, hypermotoric and ataxic movements, and certain remarkable behaviors. Those with the syndrome have a predisposition toward apparent hap...
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| Glavni autori: | , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
S. Karger AG
2012
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3366701/ https://ncbi.nlm.nih.gov/pubmed/22670133 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000328837 |
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