Your browser doesn't support javascript.
loading
Combination of whole exome sequencing and animal modeling identifies TMPRSS9 as a candidate gene for autism spectrum disorder.
Chen, Chun-An; Pal, Rituraj; Yin, Jiani; Tao, Huifang; Amawi, Abdallah; Sabo, Aniko; Bainbridge, Matthew N; Gibbs, Richard A; Zoghbi, Huda Y; Schaaf, Christian P.
Afiliación
  • Chen CA; Department of Human and Molecular Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Pal R; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX, USA.
  • Yin J; Department of Human and Molecular Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Tao H; Department of Human and Molecular Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Amawi A; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX, USA.
  • Sabo A; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX, USA.
  • Bainbridge MN; Department of Human and Molecular Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Gibbs RA; Department of Human and Molecular Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Zoghbi HY; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.
  • Schaaf CP; Rady Children's Institute for Genomic Medicine, San Diego, CA, USA.
Hum Mol Genet ; 29(3): 459-470, 2020 02 01.
Article en En | MEDLINE | ID: mdl-31943016
Asunto(s)
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastornos de Ansiedad / Serina Endopeptidasas / Codón sin Sentido / Trastorno del Espectro Autista / Secuenciación del Exoma / Proteínas de la Membrana / Trastornos de la Memoria Tipo de estudio: Etiology_studies Límite: Adolescent / Adult / Animals / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trastornos de Ansiedad / Serina Endopeptidasas / Codón sin Sentido / Trastorno del Espectro Autista / Secuenciación del Exoma / Proteínas de la Membrana / Trastornos de la Memoria Tipo de estudio: Etiology_studies Límite: Adolescent / Adult / Animals / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos