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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 PICO Portal from OpenAlex.

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

PICO Portalcitation count

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

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

PICO Portalyear

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

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

PICO Portaloa status

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

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

PICO Portaldoi

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?

PICO Portalpmid

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?

PICO Portalopenalex

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

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