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Identification of a de novo FOXP1 mutation and incidental discovery of inherited genetic variants contributing to a case of autism spectrum disorder and epilepsy.
Jay, Kristy; Mitra, Amit; Harding, Taylor; Matthes, David; Van Ness, Brian.
Afiliação
  • Jay K; College of Biological Sciences, Department of Genetics, Cell Biology, and Development, University of Minnesota-Twin Cities, Minneapolis, Minnesota.
  • Mitra A; Department of Drug Discovery and Development, Harrison School of Pharmacy, Auburn University, Auburn, Alabama.
  • Harding T; College of Biological Sciences, Department of Genetics, Cell Biology, and Development, University of Minnesota-Twin Cities, Minneapolis, Minnesota.
  • Matthes D; College of Biological Sciences, Department of Biology, Teaching, and Learning, University of Minnesota-Twin Cities, Minneapolis, Minnesota.
  • Van Ness B; College of Biological Sciences, Department of Genetics, Cell Biology, and Development, University of Minnesota-Twin Cities, Minneapolis, Minnesota.
Mol Genet Genomic Med ; 7(7): e00751, 2019 07.
Article em En | MEDLINE | ID: mdl-31111659
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Repressoras / Epilepsia / Fatores de Transcrição Forkhead / Transtorno do Espectro Autista Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Repressoras / Epilepsia / Fatores de Transcrição Forkhead / Transtorno do Espectro Autista Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adult / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article