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Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia

PaperCitations, authors & open-access status

Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia have?

ScholarIQcitation count

Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia has 60 citations in the OpenAlex counts ScholarIQ stores.

When was Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia published?

ScholarIQyear

Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia has 2015 year in the ScholarIQ index.

What is the open-access status of Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia?

ScholarIQoa status

Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia has bronze oa status in the ScholarIQ index.

What is the DOI of Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia?

ScholarIQdoi

The DOI for Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia is on the source record.

What is the PMID of Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia?

ScholarIQpmid

The PMID for Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia is on the source record.

What is the OpenAlex record for Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia?

ScholarIQopenalex

The OpenAlex for Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia is on the source record.

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