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Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation

PaperCitations, authors & open-access status

Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation have?

ScholarIQcitation count

Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation has 21 citations in the OpenAlex counts ScholarIQ stores.

When was Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation published?

ScholarIQyear

Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation has 2015 year in the ScholarIQ index.

What is the open-access status of Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation?

ScholarIQoa status

Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation has gold oa status in the ScholarIQ index.

What is the DOI of Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation?

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The DOI for Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation is on the source record.

What is the PMID of Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation?

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The PMID for Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation is on the source record.

What is the OpenAlex record for Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation?

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The OpenAlex for Case report: lupus nephritis with autoantibodies to complement alternative pathway proteins and C3 gene mutation is on the source record.

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