ID
45378
Beskrivning
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.
Länk
https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000538
Nyckelord
Versioner (2)
- 2022-11-07 2022-11-07 - Simon Heim
- 2022-12-13 2022-12-13 - Kristina Keller
Rättsinnehavare
Gail Jarvik, MD, PhD, University of Washington, Seattle, WA, USA
Uppladdad den
7 november 2022
DOI
För en begäran logga in.
Licens
Creative Commons BY 4.0
Modellkommentarer :
Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.
Itemgroup-kommentar för :
Item-kommentar för :
Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.
dbGaP phs000538 Next Generation Mendelian Genetics: Familial Combined Hyperlipidemia
Similar models
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])