ScholarIQanswers from OpenAlex

Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase

PaperCitations, authors & open-access status

Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase have?

ScholarIQcitation count

Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase has 245 citations in the OpenAlex counts ScholarIQ stores.

When was Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase published?

ScholarIQyear

Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase has 2010 year in the ScholarIQ index.

What is the open-access status of Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase?

ScholarIQoa status

Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase has green oa status in the ScholarIQ index.

What is the DOI of Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase?

ScholarIQdoi

The DOI for Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase is on the source record.

What is the PMID of Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase?

ScholarIQpmid

The PMID for Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase is on the source record.

What is the OpenAlex record for Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase?

ScholarIQopenalex

The OpenAlex for Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase is on the source record.

Related on ScholarIQ

470M+ articles · 14-day free trial