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Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability.
Torrico, Bàrbara; Fernàndez-Castillo, Noèlia; Hervás, Amaia; Milà, Montserrat; Salgado, Marta; Rueda, Isabel; Buitelaar, Jan K; Rommelse, Nanda; Oerlemans, Anoek M; Bralten, Janita; Freitag, Christine M; Reif, Andreas; Battaglia, Agatino; Mazzone, Luigi; Maestrini, Elena; Cormand, Bru; Toma, Claudio.
Afiliação
  • Torrico B; Departament de Genètica, Universitat de Barcelona, Barcelona, Spain.
  • Fernàndez-Castillo N; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Barcelona, Spain.
  • Hervás A; Institut de Biomedicina de la Universitat de Barcelona, Barcelona, Spain.
  • Milà M; Departament de Genètica, Universitat de Barcelona, Barcelona, Spain.
  • Salgado M; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Barcelona, Spain.
  • Rueda I; Institut de Biomedicina de la Universitat de Barcelona, Barcelona, Spain.
  • Buitelaar JK; Child and Adolescent Mental Health Unit, Hospital Universitari Mútua de Terrassa, Terrassa, Spain.
  • Rommelse N; Developmental Disorders Unit (UETD), Hospital Sant Joan de Déu, Esplugues de Llobregat, Spain.
  • Oerlemans AM; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Barcelona, Spain.
  • Bralten J; Biochemistry and Molecular Genetics Department, Hospital Clinic, IDIBAPS, Barcelona, Spain.
  • Freitag CM; Child and Adolescent Mental Health Unit, Hospital Universitari Mútua de Terrassa, Terrassa, Spain.
  • Reif A; Developmental Disorders Unit (UETD), Hospital Sant Joan de Déu, Esplugues de Llobregat, Spain.
  • Battaglia A; Developmental Disorders Unit (UETD), Hospital Sant Joan de Déu, Esplugues de Llobregat, Spain.
  • Mazzone L; Radboud University Medical Center, Donders Institute for Brain, Cognition and Behaviour, Department of Cognitive Neuroscience, Nijmegen, The Netherlands.
  • Maestrini E; Karakter Child and Adolescent Psychiatry University Center, Nijmegen, The Netherlands.
  • Cormand B; Karakter Child and Adolescent Psychiatry University Center, Nijmegen, The Netherlands.
  • Toma C; Radboud University Medical Center, Donders Institute for Brain, Cognition and Behaviour, Department of Psychiatry, Nijmegen, The Netherlands.
Eur J Hum Genet ; 23(12): 1694-701, 2015 Dec.
Article em En | MEDLINE | ID: mdl-25782667
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Transtorno do Espectro Autista / Proteínas de Membrana / Deficiência Intelectual Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Transtorno do Espectro Autista / Proteínas de Membrana / Deficiência Intelectual Idioma: En Ano de publicação: 2015 Tipo de documento: Article