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Missense-depleted regions in population exomes implicate ras superfamily nucleotide-binding protein alteration in patients with brain malformation.
Ge, Xiaoyan; Gong, Henry; Dumas, Kevin; Litwin, Jessica; Phillips, Joanna J; Waisfisz, Quinten; Weiss, Marjan M; Hendriks, Yvonne; Stuurman, Kyra E; Nelson, Stanley F; Grody, Wayne W; Lee, Hane; Kwok, Pui-Yan; Shieh, Joseph Tc.
Affiliation
  • Ge X; Department of Pediatrics, Division of Medical Genetics, University of California San Francisco, San Francisco, CA, USA.
  • Gong H; Institute for Human Genetics, University of California San Francisco, San Francisco, CA, USA.
  • Dumas K; Department of Pediatrics, Division of Medical Genetics, University of California San Francisco, San Francisco, CA, USA.
  • Litwin J; Institute for Human Genetics, University of California San Francisco, San Francisco, CA, USA.
  • Phillips JJ; Department of Pediatrics, Division of Medical Genetics, University of California San Francisco, San Francisco, CA, USA.
  • Waisfisz Q; Institute for Human Genetics, University of California San Francisco, San Francisco, CA, USA.
  • Weiss MM; Department of Neurology, University of California San Francisco, San Francisco, CA, USA.
  • Hendriks Y; Department of Pediatrics, University of California San Francisco, San Francisco, CA, USA.
  • Stuurman KE; Department of Neurologic Surgery, University of California San Francisco, San Francisco, CA, USA.
  • Nelson SF; Department of Pathology, University of California San Francisco, San Francisco, CA, USA.
  • Grody WW; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
  • Lee H; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
  • Kwok PY; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
  • Shieh JT; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
Article in En | MEDLINE | ID: mdl-28868155

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: NPJ Genom Med Year: 2016 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: NPJ Genom Med Year: 2016 Document type: Article Affiliation country: Country of publication: