Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia is a paper indexed in PICO Portal from OpenAlex.
How many citations does Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia have?
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia has 445 citations in the OpenAlex counts PICO Portal stores.
When was Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia published?
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia has 2010 year in the PICO Portal index.
What is the open-access status of Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia?
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia has closed oa status in the PICO Portal index.
What is the DOI of Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia?
The DOI for Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia is on the source record.
What is the PMID of Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia?
The PMID for Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia is on the source record.
What is the OpenAlex record for Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia?
The OpenAlex for Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia is on the source record.