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MeCP2_e2 partially compensates for lack of MeCP2_e1: A male case of Rett syndrome.
Takeguchi, Ryo; Takahashi, Satoru; Kuroda, Mami; Tanaka, Ryosuke; Suzuki, Nao; Tomonoh, Yuko; Ihara, Yukiko; Sugiyama, Nobuyoshi; Itoh, Masayuki.
Afiliación
  • Takeguchi R; Department of Pediatrics, Asahikawa Medical University, Hokkaido, Japan.
  • Takahashi S; Department of Pediatrics, Asahikawa Medical University, Hokkaido, Japan.
  • Kuroda M; Department of Pediatrics, Asahikawa Medical University, Hokkaido, Japan.
  • Tanaka R; Department of Pediatrics, Asahikawa Medical University, Hokkaido, Japan.
  • Suzuki N; Department of Pediatrics, Asahikawa Medical University, Hokkaido, Japan.
  • Tomonoh Y; Department of Pediatrics, Fukuoka University, Fukuoka, Japan.
  • Ihara Y; Department of Pediatrics, Fukuoka University, Fukuoka, Japan.
  • Sugiyama N; Department of Pediatrics, Tokai University, Kanagawa, Japan.
  • Itoh M; Department of Mental Retardation and Birth Defect Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan.
Mol Genet Genomic Med ; 8(2): e1088, 2020 02.
Article en En | MEDLINE | ID: mdl-31816669
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Rett / Proteína 2 de Unión a Metil-CpG Tipo de estudio: Prognostic_studies Límite: Child / Humans / Male Idioma: En Revista: Mol Genet Genomic Med Año: 2020 Tipo del documento: Article País de afiliación: Japón
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Rett / Proteína 2 de Unión a Metil-CpG Tipo de estudio: Prognostic_studies Límite: Child / Humans / Male Idioma: En Revista: Mol Genet Genomic Med Año: 2020 Tipo del documento: Article País de afiliación: Japón