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A rare genetic variant in the cleavage site of prepro-orexin is associated with idiopathic hypersomnia

PaperCitations, authors & open-access status

A rare genetic variant in the cleavage site of prepro-orexin is associated with idiopathic hypersomnia is a paper indexed in ScholarIQ from OpenAlex.

How many citations does A rare genetic variant in the cleavage site of prepro-orexin is associated with idiopathic hypersomnia have?

ScholarIQcitation count

A rare genetic variant in the cleavage site of prepro-orexin is associated with idiopathic hypersomnia has 21 citations in the OpenAlex counts ScholarIQ stores.

When was A rare genetic variant in the cleavage site of prepro-orexin is associated with idiopathic hypersomnia published?

ScholarIQyear

A rare genetic variant in the cleavage site of prepro-orexin is associated with idiopathic hypersomnia has 2022 year in the ScholarIQ index.

What is the open-access status of A rare genetic variant in the cleavage site of prepro-orexin is associated with idiopathic hypersomnia?

ScholarIQoa status

A rare genetic variant in the cleavage site of prepro-orexin is associated with idiopathic hypersomnia has gold oa status in the ScholarIQ index.

What is the DOI of A rare genetic variant in the cleavage site of prepro-orexin is associated with idiopathic hypersomnia?

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What is the PMID of A rare genetic variant in the cleavage site of prepro-orexin is associated with idiopathic hypersomnia?

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The OpenAlex for A rare genetic variant in the cleavage site of prepro-orexin is associated with idiopathic hypersomnia is on the source record.

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