ID
45034
Description
Principal Investigator: Junko Oshima, MD, PhD, Department of Pathology, University of Washington, Seattle, WA, USA MeSH: Werner Syndrome https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000434 Werner syndrome (WS) is an adult-onset progeroid syndrome characterized by accelerated aging. The International Registry of Werner Syndrome in the Department of Pathology, University of Washington, collects WS cases from all over the world. Classical WS is caused by WRN mutations. Those who do not carry *WRN* are categorized as "atypical Werner syndrome." A small subset of atypical WS is caused by *LMNA* mutations. There also are many cases whose causes are still unknown. The purpose of this study is to identify other causative gene(s) of atypical WS.
Lien
https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000434
Mots-clés
Versions (2)
- 29/07/2022 29/07/2022 - Simon Heim
- 12/10/2022 12/10/2022 - Adrian Schulz
Détendeur de droits
Junko Oshima, MD, PhD, Department of Pathology, University of Washington, Seattle, WA, USA
Téléchargé le
29 juillet 2022
DOI
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Licence
Creative Commons BY 4.0
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dbGaP phs000434 Next Generation Mendelian Genetics: Atypical Werner Syndrome
Similar models
Eligibility Criteria
C1711435 (UMLS CUI [1,2])
C0524459 (UMLS CUI [1,3])
C0026882 (UMLS CUI [1,4])
C1512693 (UMLS CUI [2,1])
C0043119 (UMLS CUI [2,2])