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Novel FOXG1 mutations associated with the congenital variant of Rett syndrome.
Mencarelli, M A; Spanhol-Rosseto, A; Artuso, R; Rondinella, D; De Filippis, R; Bahi-Buisson, N; Nectoux, J; Rubinsztajn, R; Bienvenu, T; Moncla, A; Chabrol, B; Villard, L; Krumina, Z; Armstrong, J; Roche, A; Pineda, M; Gak, E; Mari, F; Ariani, F; Renieri, A.
Affiliation
  • Mencarelli MA; Medical Genetics, Molecular Biology Department, University of Siena, 53100 Siena, Italy.
J Med Genet ; 47(1): 49-53, 2010 Jan.
Article in En | MEDLINE | ID: mdl-19578037
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Full text: 1 Database: MEDLINE Main subject: Rett Syndrome / Methyl-CpG-Binding Protein 2 / Forkhead Transcription Factors / Nerve Tissue Proteins Type of study: Prognostic_studies / Risk_factors_studies Limits: Child, preschool / Female / Humans Language: En Year: 2010 Type: Article
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Full text: 1 Database: MEDLINE Main subject: Rett Syndrome / Methyl-CpG-Binding Protein 2 / Forkhead Transcription Factors / Nerve Tissue Proteins Type of study: Prognostic_studies / Risk_factors_studies Limits: Child, preschool / Female / Humans Language: En Year: 2010 Type: Article