ScholarIQanswers from OpenAlex

A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy

PaperCitations, authors & open-access status

A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy is a paper indexed in ScholarIQ from OpenAlex.

How many citations does A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy have?

ScholarIQcitation count

A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy has 316 citations in the OpenAlex counts ScholarIQ stores.

When was A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy published?

ScholarIQyear

A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy has 2014 year in the ScholarIQ index.

What is the open-access status of A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy?

ScholarIQoa status

A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy has green oa status in the ScholarIQ index.

What is the DOI of A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy?

ScholarIQdoi

The DOI for A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy is on the source record.

What is the PMID of A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy?

ScholarIQpmid

The PMID for A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy is on the source record.

What is the OpenAlex record for A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy?

ScholarIQopenalex

The OpenAlex for A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy is on the source record.

Related on ScholarIQ

470M+ articles · 14-day free trial