ScholarIQanswers from OpenAlex

INF2 mutations cause kidney disease through a gain-of-function mechanism

PaperCitations, authors & open-access status

INF2 mutations cause kidney disease through a gain-of-function mechanism is a paper indexed in ScholarIQ from OpenAlex.

How many citations does INF2 mutations cause kidney disease through a gain-of-function mechanism have?

ScholarIQcitation count

INF2 mutations cause kidney disease through a gain-of-function mechanism has 15 citations in the OpenAlex counts ScholarIQ stores.

When was INF2 mutations cause kidney disease through a gain-of-function mechanism published?

ScholarIQyear

INF2 mutations cause kidney disease through a gain-of-function mechanism has 2024 year in the ScholarIQ index.

What is the open-access status of INF2 mutations cause kidney disease through a gain-of-function mechanism?

ScholarIQoa status

INF2 mutations cause kidney disease through a gain-of-function mechanism has gold oa status in the ScholarIQ index.

What is the DOI of INF2 mutations cause kidney disease through a gain-of-function mechanism?

ScholarIQdoi

The DOI for INF2 mutations cause kidney disease through a gain-of-function mechanism is on the source record.

What is the PMID of INF2 mutations cause kidney disease through a gain-of-function mechanism?

ScholarIQpmid

The PMID for INF2 mutations cause kidney disease through a gain-of-function mechanism is on the source record.

What is the OpenAlex record for INF2 mutations cause kidney disease through a gain-of-function mechanism?

ScholarIQopenalex

The OpenAlex for INF2 mutations cause kidney disease through a gain-of-function mechanism is on the source record.

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