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Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders.
Sollis, Elliot; Deriziotis, Pelagia; Saitsu, Hirotomo; Miyake, Noriko; Matsumoto, Naomichi; Hoffer, Mariëtte J V; Ruivenkamp, Claudia A L; Alders, Mariëlle; Okamoto, Nobuhiko; Bijlsma, Emilia K; Plomp, Astrid S; Fisher, Simon E.
Afiliação
  • Sollis E; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.
  • Deriziotis P; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.
  • Saitsu H; Department of Biochemistry, Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Miyake N; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Matsumoto N; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Hoffer MJV; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Ruivenkamp CAL; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Alders M; Department of Clinical Genetics, Academic Medical Center, Amsterdam, The Netherlands.
  • Okamoto N; Department of Medical Genetics, Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka, Japan.
  • Bijlsma EK; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Plomp AS; Department of Clinical Genetics, Academic Medical Center, Amsterdam, The Netherlands.
  • Fisher SE; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.
Hum Mutat ; 38(11): 1542-1554, 2017 11.
Article em En | MEDLINE | ID: mdl-28741757
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Proteínas Repressoras / Deficiências do Desenvolvimento / Mutação de Sentido Incorreto / Fatores de Transcrição Forkhead Idioma: En Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Holanda
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fenótipo / Proteínas Repressoras / Deficiências do Desenvolvimento / Mutação de Sentido Incorreto / Fatores de Transcrição Forkhead Idioma: En Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Holanda