Your browser doesn't support javascript.
loading
Bridging the splicing gap in human genetics with long-read RNA sequencing: finding the protein isoform drivers of disease.
Castaldi, Peter J; Abood, Abdullah; Farber, Charles R; Sheynkman, Gloria M.
  • Castaldi PJ; Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA 02115, USA.
  • Abood A; Division of General Medicine and Primary Care, Department of Medicine, Brigham and Women's Hospital, Boston, MA 02115, USA.
  • Farber CR; Center for Public Health Genomics, School of Medicine, University of Virginia, Charlottesville, VA 22903, USA.
  • Sheynkman GM; Department of Biochemistry and Molecular Genetics, School of Medicine, University of Virginia, Charlottesville, VA 22903, USA.
Hum Mol Genet ; 31(R1): R123-R136, 2022 10 20.
Article en En | MEDLINE | ID: mdl-35960994
Asunto(s)
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Isoformas de ARN / Genética Humana Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Isoformas de ARN / Genética Humana Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article