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A possibly new autoinflammatory disease due to compound heterozygous phosphomevalonate kinase gene mutation

PaperCitations, authors & open-access status

A possibly new autoinflammatory disease due to compound heterozygous phosphomevalonate kinase gene mutation is a paper indexed in ScholarIQ from OpenAlex.

How many citations does A possibly new autoinflammatory disease due to compound heterozygous phosphomevalonate kinase gene mutation have?

ScholarIQcitation count

A possibly new autoinflammatory disease due to compound heterozygous phosphomevalonate kinase gene mutation has 14 citations in the OpenAlex counts ScholarIQ stores.

When was A possibly new autoinflammatory disease due to compound heterozygous phosphomevalonate kinase gene mutation published?

ScholarIQyear

A possibly new autoinflammatory disease due to compound heterozygous phosphomevalonate kinase gene mutation has 2022 year in the ScholarIQ index.

What is the open-access status of A possibly new autoinflammatory disease due to compound heterozygous phosphomevalonate kinase gene mutation?

ScholarIQoa status

A possibly new autoinflammatory disease due to compound heterozygous phosphomevalonate kinase gene mutation has closed oa status in the ScholarIQ index.

What is the DOI of A possibly new autoinflammatory disease due to compound heterozygous phosphomevalonate kinase gene mutation?

ScholarIQdoi

The DOI for A possibly new autoinflammatory disease due to compound heterozygous phosphomevalonate kinase gene mutation is on the source record.

What is the PMID of A possibly new autoinflammatory disease due to compound heterozygous phosphomevalonate kinase gene mutation?

ScholarIQpmid

The PMID for A possibly new autoinflammatory disease due to compound heterozygous phosphomevalonate kinase gene mutation is on the source record.

What is the OpenAlex record for A possibly new autoinflammatory disease due to compound heterozygous phosphomevalonate kinase gene mutation?

ScholarIQopenalex

The OpenAlex for A possibly new autoinflammatory disease due to compound heterozygous phosphomevalonate kinase gene mutation is on the source record.

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