Skip to content
PICO Portalanswers from OpenAlex

Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans

PaperCitations, authors & open-access status

Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans is a paper indexed in PICO Portal from OpenAlex.

How many citations does Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans have?

PICO Portalcitation count

Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans has 233 citations in the OpenAlex counts PICO Portal stores.

When was Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans published?

PICO Portalyear

Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans has 2013 year in the PICO Portal index.

What is the open-access status of Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans?

PICO Portaloa status

Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans has hybrid oa status in the PICO Portal index.

What is the DOI of Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans?

PICO Portaldoi

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?

PICO Portalpmid

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?

PICO Portalopenalex

The OpenAlex for Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans is on the source record.

Related on PICO Portal

470M+ articles · 14-day free trial