The diagnosis of Angelman syndrome (AS) can be con®rmed by genetic laboratory in about 80% of cases. In 20%, the diagnosis remains clinical, but often there is uncertainty about the correctness of the clinical diagnosis and alternative diagnosis may be investigated. In evaluating individuals for AS
Angelman syndrome: Correlations between epilepsy phenotypes and genotypes
✍ Scribed by Berge A. Minassian; Timothy M. Delorey; Richard W. Olsen; Michel Philippart; Yuri Bronstein; Quanwei Zhang; Renzo Guerrini; Paul van Ness; Marie O. Livet; Dr Antonio V. Delgado-Escueta
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 819 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0364-5134
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