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Mixed Neurodevelopmental and Neurodegenerative Pathology in Nhe6-Null Mouse Model of Christianson Syndrome.
Xu, Meiyu; Ouyang, Qing; Gong, Jingyi; Pescosolido, Matthew F; Pruett, Brandon S; Mishra, Sasmita; Schmidt, Michael; Jones, Richard N; Gamsiz Uzun, Ece D; Lizarraga, Sofia B; Morrow, Eric M.
Afiliação
  • Xu M; Department of Molecular Biology, Cell Biology and Biochemistry, Brown University, Providence, RI 02912.
  • Ouyang Q; Brown Institute for Brain Science, Brown University, Providence, RI 02912.
  • Gong J; Developmental Disorders Genetics Research Program, Emma Pendleton Bradley Hospital, East Providence, RI 02915.
  • Pescosolido MF; Department of Molecular Biology, Cell Biology and Biochemistry, Brown University, Providence, RI 02912.
  • Pruett BS; Brown Institute for Brain Science, Brown University, Providence, RI 02912.
  • Mishra S; Developmental Disorders Genetics Research Program, Emma Pendleton Bradley Hospital, East Providence, RI 02915.
  • Schmidt M; Department of Molecular Biology, Cell Biology and Biochemistry, Brown University, Providence, RI 02912.
  • Jones RN; Brown Institute for Brain Science, Brown University, Providence, RI 02912.
  • Gamsiz Uzun ED; Department of Molecular Biology, Cell Biology and Biochemistry, Brown University, Providence, RI 02912.
  • Lizarraga SB; Brown Institute for Brain Science, Brown University, Providence, RI 02912.
  • Morrow EM; Developmental Disorders Genetics Research Program, Emma Pendleton Bradley Hospital, East Providence, RI 02915.
eNeuro ; 4(6)2017.
Article em En | MEDLINE | ID: mdl-29349289
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ataxia / Encéfalo / Transtornos da Motilidade Ocular / Trocadores de Sódio-Hidrogênio / Doenças Genéticas Ligadas ao Cromossomo X / Epilepsia / Deficiência Intelectual / Microcefalia / Degeneração Neural Limite: Animals Idioma: En Revista: ENeuro Ano de publicação: 2017 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ataxia / Encéfalo / Transtornos da Motilidade Ocular / Trocadores de Sódio-Hidrogênio / Doenças Genéticas Ligadas ao Cromossomo X / Epilepsia / Deficiência Intelectual / Microcefalia / Degeneração Neural Limite: Animals Idioma: En Revista: ENeuro Ano de publicação: 2017 Tipo de documento: Article