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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 PICO Portal from OpenAlex.

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

PICO Portalcitation count

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

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

PICO Portalyear

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

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

PICO Portaloa status

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

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

PICO Portaldoi

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?

PICO Portalpmid

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?

PICO Portalopenalex

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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