MECP2 gene mutations in twenty-six cases with atypical Rett syndrome
OBJECTIVE: Rett syndrome (RTT) is an X-linked progressive neurodeveopmental disorder that almost exclusively affects girls, and is one of the most common causes of mental retardation in females, with an estimated prevalence of approximately 1 in 10,000 - 15,000 female individuals. Mutations in X-lin...
| Publié dans: | Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 44(2006), 4 vom: 19. Apr., Seite 285-8 |
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| Auteur principal: | |
| Autres auteurs: | , , , , |
| Format: | Article |
| Langue: | Chinese |
| Publié: |
2006
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| Accès à la collection: | Zhonghua er ke za zhi = Chinese journal of pediatrics |
| Sujets: | English Abstract Journal Article MECP2 protein, human Methyl-CpG-Binding Protein 2 |