ID
45378
Description
Principal Investigator: Gail Jarvik, MD, PhD, University of Washington, Seattle, WA, USA MeSH: Hyperlipidemia, Familial Combined https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000538 The NHGRI Next Generation Mendelian Genetics project uses exome resequencing to identify variants in unsolved Mendelian diseases. The research study procedures included the collection of a fasting blood sample, 2 medical history/life style questionnaires and a measurement of subjects' waist circumference that were completed many years ago. Blood samples were analyzed for metabolic markers including cholesterol, HDL, triglycerides and APOE. Genetic tests targeted known and novel genes and polymorphisms associated with carotid artery disease.
Lien
https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000538
Mots-clés
Versions (2)
- 07/11/2022 07/11/2022 - Simon Heim
- 13/12/2022 13/12/2022 - Kristina Keller
Détendeur de droits
Gail Jarvik, MD, PhD, University of Washington, Seattle, WA, USA
Téléchargé le
7 de novembro de 2022
DOI
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Licence
Creative Commons BY 4.0
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dbGaP phs000538 Next Generation Mendelian Genetics: Familial Combined Hyperlipidemia
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Eligibility Criteria
C0680251 (UMLS CUI [1,2])
C0023820 (UMLS CUI [1,2])
C3163633 (UMLS CUI [1,2])
C0023820 (UMLS CUI [1,3])
C0241889 (UMLS CUI [1,2])
C0007222 (UMLS CUI [1,3])