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Regulatory de novo mutations underlying intellectual disability.
De Vas, Matias G; Boulet, Fanny; Joshi, Shweta S; Garstang, Myles G; Khan, Tahir N; Atla, Goutham; Parry, David; Moore, David; Cebola, Inês; Zhang, Shuchen; Cui, Wei; Lampe, Anne K; Lam, Wayne W; Ferrer, Jorge; Pradeepa, Madapura M; Atanur, Santosh S.
Afiliação
  • De Vas MG; Section of Genetics and Genomics, Department of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
  • Boulet F; Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • Joshi SS; Section of Genetics and Genomics, Department of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
  • Garstang MG; Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • Khan TN; School of Biological Sciences, University of Essex, Colchester, UK.
  • Atla G; Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • Parry D; Department of Biological Sciences, National University of Medical Sciences, Rawalpindi, Pakistan.
  • Moore D; Section of Genetics and Genomics, Department of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
  • Cebola I; Regulatory Genomics and Diabetes, Centre for Genomic Regulation, The Barcelona Institute of Science and Technology, Barcelona, Spain.
  • Zhang S; Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas, Barcelona, Spain.
  • Cui W; MRC Human Genetics Unit, University of Edinburgh, Edinburgh, UK.
  • Lampe AK; South-East Scotland Regional Genetics Service, Western General Hospital, Edinburgh, UK.
  • Lam WW; Section of Genetics and Genomics, Department of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
  • Ferrer J; Institute of Reproductive and Developmental Biology, Faculty of Medicine, Imperial College London, London, UK.
  • Pradeepa MM; South-East Scotland Regional Genetics Service, Western General Hospital, Edinburgh, UK.
  • Atanur SS; South-East Scotland Regional Genetics Service, Western General Hospital, Edinburgh, UK.
Life Sci Alliance ; 6(5)2023 05.
Article em En | MEDLINE | ID: mdl-36854624
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Deficiência Intelectual Limite: Adult / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Deficiência Intelectual Limite: Adult / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article