MECP2 gene mutations in twenty-six cases with atypical Rett syndrome

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...

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Bibliographische Detailangaben
Veröffentlicht in:Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 44(2006), 4 vom: 19. Apr., Seite 285-8
1. Verfasser: Li, Mei-rong (VerfasserIn)
Weitere Verfasser: Pan, Hong, Bao, Xin-hua, Zhang, Yu-zhi, Jiang, Sheng-ling, Wu, Xi-ru
Format: Aufsatz
Sprache:Chinese
Veröffentlicht: 2006
Zugriff auf das übergeordnete Werk:Zhonghua er ke za zhi = Chinese journal of pediatrics
Schlagworte:English Abstract Journal Article MECP2 protein, human Methyl-CpG-Binding Protein 2