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Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans

PaperCitations, authors & open-access status

Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans have?

ScholarIQcitation count

Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans has 231 citations in the OpenAlex counts ScholarIQ stores.

When was Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans published?

ScholarIQyear

Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans has 2014 year in the ScholarIQ index.

What is the open-access status of Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans?

ScholarIQoa status

Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans has closed oa status in the ScholarIQ index.

What is the DOI of Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans?

ScholarIQdoi

The DOI for Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans is on the source record.

What is the PMID of Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans?

ScholarIQpmid

The PMID for Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans is on the source record.

What is the OpenAlex record for Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans?

ScholarIQopenalex

The OpenAlex for Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans is on the source record.

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