ScholarIQanswers from OpenAlex

Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type

PaperCitations, authors & open-access status

Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type have?

ScholarIQcitation count

Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type has 26 citations in the OpenAlex counts ScholarIQ stores.

When was Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type published?

ScholarIQyear

Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type has 2022 year in the ScholarIQ index.

What is the open-access status of Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type?

ScholarIQoa status

Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type has gold oa status in the ScholarIQ index.

What is the DOI of Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type?

ScholarIQdoi

The DOI for Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type is on the source record.

What is the PMID of Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type?

ScholarIQpmid

The PMID for Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type is on the source record.

What is the OpenAlex record for Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type?

ScholarIQopenalex

The OpenAlex for Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type is on the source record.

Related on ScholarIQ

470M+ articles · 14-day free trial