Rett syndrome: clinical and molecular characterization of two Brazilian patients Síndrome de Rett: caracterização clínica e molecular de dois casos brasileiros

BACKGROUND: Rett syndrome (RS) is recognized as a pan-ethnic condition. Since the identification of mutations in the MECP2 gene, more patients have been diagnosed, and a broad spectrum of phenotypes has been reported. There is a lack of phenotype-genotype studies. OBJECTIVE: To describe two cases of...

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Bibliográfalaš dieđut

Váldodahkkit:	Andrea Stachon, Francisco Baptista Assumpção Jr, Salmo Raskin
Materiálatiipa:	Artigo
Giella:	Inglês
Almmustuhtton:	Thieme Revinter Publicações 2007-03-01
Ráidu:	Arquivos de Neuro-Psiquiatria
Fáttát:	síndrome de Rett MECP2 mutação Brasil Rett syndrome MECP2 mutations Brazilian cases
Liŋkkat:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2007000100009
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