Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans
Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans is a paper indexed in ScholarIQ from OpenAlex.
How many citations does Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans have?
Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans has 233 citations in the OpenAlex counts ScholarIQ stores.
When was Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans published?
Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans has 2013 year in the ScholarIQ index.
What is the open-access status of Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans?
Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans has hybrid oa status in the ScholarIQ index.
What is the DOI of Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans?
The DOI for Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans is on the source record.
What is the PMID of Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans?
The PMID for Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans is on the source record.
What is the OpenAlex record for Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans?
The OpenAlex for Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans is on the source record.