Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies

Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies have?

Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies has 80 citations in the OpenAlex counts ScholarIQ stores.

When was Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies published?

Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies has 2017 year in the ScholarIQ index.

What is the open-access status of Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies?

Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies has closed oa status in the ScholarIQ index.

What is the DOI of Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies?

The DOI for Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies is on the source record.

What is the PMID of Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies?

The PMID for Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies is on the source record.

What is the OpenAlex record for Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies?

The OpenAlex for Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies is on the source record.