STUDY: Next Generation Mendelian Genetics: Atypical Werner Syndrome

Study Description

Werner syndrome (WS) is an adult-onset progeroid syndrome characterized by accelerated aging. The International Registry of Werner... Show More

Study Accession Alternative Stable ID type
phs000434.v1.p1 dbGaP Case Set

Who controls access to this study

National Human Genome Research Institute
Access information:

Publications

8602509
20443122
12927431

Data provider(s)

  • Title Name Institute
    Principal Investigators Junko Oshima, MD, PhD Department of Pathology, University of Washington, Seattle, WA, USA
    Principal Investigators George M. Martin MD Department of Pathology, University of Washington, Seattle, WA, USA
    Funding Source R24 CA78088 International Registry of Werner Syndrome
    Sequencing Center Northwest Genomics Center (NWGC; Director: Deborah Nickerson) University of Washington, Seattle, WA, USA
    Funding Source for Sequencing HG005608 National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA

Who archives the data?

The database of Genotypes and Phenotypes (dbGaP)