## Abstract Rett syndrome is a neurodevelopmental disorder that represents one of the most common genetic causes of mental retardation in girls. __MECP2__ point mutations in exons 2โ4 account for about 80% of classic Rett cases and for a lower percentage of variant patients. We investigated the gen
โฆ LIBER โฆ
P31.9 Genotype-phenotype correlation in Rett syndrome (EEG investigation)
โ Scribed by N. Gorbachevskaya; V. Voinova-Ulas; A. Sorokin; I. Iourov; A. Boudilov; L. Giunti; L. Villar; M. Giovanucci-Uzielli; Yu Yurov; S. Vorsanova
- Book ID
- 118433745
- Publisher
- Elsevier Science
- Year
- 2006
- Tongue
- English
- Weight
- 42 KB
- Volume
- 117
- Category
- Article
- ISSN
- 1388-2457
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