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Aberrant mitochondrial function in patient-derived neural cells from CDKL5 deficiency disorder and Rett syndrome.
Jagtap, Smita; Thanos, Jessica M; Fu, Ting; Wang, Jennifer; Lalonde, Jasmin; Dial, Thomas O; Feiglin, Ariel; Chen, Jeffrey; Kohane, Isaac; Lee, Jeannie T; Sheridan, Steven D; Perlis, Roy H.
Afiliação
  • Jagtap S; Center for Quantitative Health, Center for Genomic Medicine, and Department of Psychiatry, Massachusetts General Hospital, Boston, MA 02114, USA.
  • Thanos JM; Department of Psychiatry, Harvard Medical School, Boston, MA 02115, USA.
  • Fu T; Center for Quantitative Health, Center for Genomic Medicine, and Department of Psychiatry, Massachusetts General Hospital, Boston, MA 02114, USA.
  • Wang J; Department of Psychiatry, Harvard Medical School, Boston, MA 02115, USA.
  • Lalonde J; Center for Quantitative Health, Center for Genomic Medicine, and Department of Psychiatry, Massachusetts General Hospital, Boston, MA 02114, USA.
  • Dial TO; Department of Psychiatry, Harvard Medical School, Boston, MA 02115, USA.
  • Feiglin A; Center for Quantitative Health, Center for Genomic Medicine, and Department of Psychiatry, Massachusetts General Hospital, Boston, MA 02114, USA.
  • Chen J; Department of Psychiatry, Harvard Medical School, Boston, MA 02115, USA.
  • Kohane I; Department of Molecular and Cellular Biology, University of Guelph, Guelph, ON, Canada N1G 2W1.
  • Lee JT; Howard Hughes Medical Institute, Massachusetts General Hospital, Boston, MA 02114, USA.
  • Sheridan SD; Department of Molecular Biology, Massachusetts General Hospital, Boston, MA 02114, USA.
  • Perlis RH; Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.
Hum Mol Genet ; 28(21): 3625-3636, 2019 11 01.
Article em En | MEDLINE | ID: mdl-31518399
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Espasmos Infantis / Síndrome de Rett / Síndromes Epilépticas / Mitocôndrias Limite: Adult / Child, preschool / Female / Humans Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
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PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Espasmos Infantis / Síndrome de Rett / Síndromes Epilépticas / Mitocôndrias Limite: Adult / Child, preschool / Female / Humans Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos