Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype
Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype is a paper indexed in ScholarIQ from OpenAlex.
How many citations does Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype have?
Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype has 220 citations in the OpenAlex counts ScholarIQ stores.
When was Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype published?
Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype has 2003 year in the ScholarIQ index.
What is the open-access status of Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype?
Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype has closed oa status in the ScholarIQ index.
What is the DOI of Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype?
The DOI for Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype is on the source record.
What is the PMID of Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype?
The PMID for Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype is on the source record.
What is the OpenAlex record for Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype?
The OpenAlex for Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype is on the source record.