Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation
Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation is a paper indexed in ScholarIQ from OpenAlex.
How many citations does Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation have?
Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation has 63 citations in the OpenAlex counts ScholarIQ stores.
When was Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation published?
Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation has 2013 year in the ScholarIQ index.
What is the open-access status of Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation?
Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation has closed oa status in the ScholarIQ index.
What is the DOI of Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation?
The DOI for Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation is on the source record.
What is the PMID of Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation?
The PMID for Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation is on the source record.
What is the OpenAlex record for Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation?
The OpenAlex for Distinct neurological features in a patient with Schinzel–Giedion syndrome caused by a recurrent SETBP1 mutation is on the source record.