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Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy.
Corbett, Mark A; van Eyk, Clare L; Webber, Dani L; Bent, Stephen J; Newman, Morgan; Harper, Kelly; Berry, Jesia G; Azmanov, Dimitar N; Woodward, Karen J; Gardner, Alison E; Slee, Jennie; Pérez-Jurado, Luís A; MacLennan, Alastair H; Gecz, Jozef.
Affiliation
  • Corbett MA; 1Robinson Research Institute & Adelaide Medical School, University of Adelaide, Adelaide, South Australia 5000 Australia.
  • van Eyk CL; 1Robinson Research Institute & Adelaide Medical School, University of Adelaide, Adelaide, South Australia 5000 Australia.
  • Webber DL; 1Robinson Research Institute & Adelaide Medical School, University of Adelaide, Adelaide, South Australia 5000 Australia.
  • Bent SJ; Data61, Commonwealth Scientific and Industrial Research Organisation, Ecosciences Precinct, Dutton Park, Brisbane, QLD 4102 Australia.
  • Newman M; 3School of Biological Sciences, University of Adelaide, Adelaide, South Australia 5005 Australia.
  • Harper K; 1Robinson Research Institute & Adelaide Medical School, University of Adelaide, Adelaide, South Australia 5000 Australia.
  • Berry JG; 1Robinson Research Institute & Adelaide Medical School, University of Adelaide, Adelaide, South Australia 5000 Australia.
  • Azmanov DN; 4Department of Diagnostic Genomics, Queen Elizabeth II Medical Centre, PathWest, Nedlands, WA 6009 Australia.
  • Woodward KJ; 4Department of Diagnostic Genomics, Queen Elizabeth II Medical Centre, PathWest, Nedlands, WA 6009 Australia.
  • Gardner AE; 5School of Biomedical Sciences, University of Western Australia, Perth, WA 6009 Australia.
  • Slee J; 1Robinson Research Institute & Adelaide Medical School, University of Adelaide, Adelaide, South Australia 5000 Australia.
  • Pérez-Jurado LA; 6Genetic Services of Western Australia, King Edward Memorial Hospital, Subiaco, WA 6008 Australia.
  • MacLennan AH; 7Genetics Unit, Universitat Pompeu Fabra, Barcelona, 08003 Spain.
  • Gecz J; Hospital del Mar Research Institute (IMIM) and Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Barcelona, 08003 Spain.
NPJ Genom Med ; 3: 33, 2018.
Article in En | MEDLINE | ID: mdl-30564460
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: NPJ Genom Med Year: 2018 Document type: Article Country of publication:
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: NPJ Genom Med Year: 2018 Document type: Article Country of publication: