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Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy

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Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy have?

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Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy has 32 citations in the OpenAlex counts ScholarIQ stores.

When was Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy published?

ScholarIQyear

Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy has 2020 year in the ScholarIQ index.

What is the open-access status of Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy?

ScholarIQoa status

Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy has hybrid oa status in the ScholarIQ index.

What is the DOI of Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy?

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The DOI for Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy is on the source record.

What is the PMID of Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy?

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The PMID for Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy is on the source record.

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The OpenAlex for Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy is on the source record.

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