ScholarIQanswers from OpenAlex

Genotype–phenotype correlation in seven motor neuron disease families with novel <scp><i>ALS2</i></scp> mutations

PaperCitations, authors & open-access status

Genotype–phenotype correlation in seven motor neuron disease families with novel <scp><i>ALS2</i></scp> mutations is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Genotype–phenotype correlation in seven motor neuron disease families with novel <scp><i>ALS2</i></scp> mutations have?

ScholarIQcitation count

Genotype–phenotype correlation in seven motor neuron disease families with novel <scp><i>ALS2</i></scp> mutations has 30 citations in the OpenAlex counts ScholarIQ stores.

When was Genotype–phenotype correlation in seven motor neuron disease families with novel <scp><i>ALS2</i></scp> mutations published?

ScholarIQyear

Genotype–phenotype correlation in seven motor neuron disease families with novel <scp><i>ALS2</i></scp> mutations has 2020 year in the ScholarIQ index.

What is the open-access status of Genotype–phenotype correlation in seven motor neuron disease families with novel <scp><i>ALS2</i></scp> mutations?

ScholarIQoa status

Genotype–phenotype correlation in seven motor neuron disease families with novel <scp><i>ALS2</i></scp> mutations has hybrid oa status in the ScholarIQ index.

What is the DOI of Genotype–phenotype correlation in seven motor neuron disease families with novel <scp><i>ALS2</i></scp> mutations?

ScholarIQdoi

The DOI for Genotype–phenotype correlation in seven motor neuron disease families with novel <scp><i>ALS2</i></scp> mutations is on the source record.

What is the PMID of Genotype–phenotype correlation in seven motor neuron disease families with novel <scp><i>ALS2</i></scp> mutations?

ScholarIQpmid

The PMID for Genotype–phenotype correlation in seven motor neuron disease families with novel <scp><i>ALS2</i></scp> mutations is on the source record.

What is the OpenAlex record for Genotype–phenotype correlation in seven motor neuron disease families with novel <scp><i>ALS2</i></scp> mutations?

ScholarIQopenalex

The OpenAlex for Genotype–phenotype correlation in seven motor neuron disease families with novel <scp><i>ALS2</i></scp> mutations is on the source record.

Related on ScholarIQ

470M+ articles · 14-day free trial