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Infantile Neurodegenerative Disorder Associated with Mutations in<i>TBCD</i>, an Essential Gene in the Tubulin Heterodimer Assembly Pathway

PaperCitations, authors & open-access status

Infantile Neurodegenerative Disorder Associated with Mutations in<i>TBCD</i>, an Essential Gene in the Tubulin Heterodimer Assembly Pathway is a paper indexed in PICO Portal from OpenAlex.

How many citations does Infantile Neurodegenerative Disorder Associated with Mutations in<i>TBCD</i>, an Essential Gene in the Tubulin Heterodimer Assembly Pathway have?

PICO Portalcitation count

Infantile Neurodegenerative Disorder Associated with Mutations in<i>TBCD</i>, an Essential Gene in the Tubulin Heterodimer Assembly Pathway has 25 citations in the OpenAlex counts PICO Portal stores.

When was Infantile Neurodegenerative Disorder Associated with Mutations in<i>TBCD</i>, an Essential Gene in the Tubulin Heterodimer Assembly Pathway published?

PICO Portalyear

Infantile Neurodegenerative Disorder Associated with Mutations in<i>TBCD</i>, an Essential Gene in the Tubulin Heterodimer Assembly Pathway has 2016 year in the PICO Portal index.

What is the open-access status of Infantile Neurodegenerative Disorder Associated with Mutations in<i>TBCD</i>, an Essential Gene in the Tubulin Heterodimer Assembly Pathway?

PICO Portaloa status

Infantile Neurodegenerative Disorder Associated with Mutations in<i>TBCD</i>, an Essential Gene in the Tubulin Heterodimer Assembly Pathway has bronze oa status in the PICO Portal index.

What is the DOI of Infantile Neurodegenerative Disorder Associated with Mutations in<i>TBCD</i>, an Essential Gene in the Tubulin Heterodimer Assembly Pathway?

PICO Portaldoi

The DOI for Infantile Neurodegenerative Disorder Associated with Mutations in<i>TBCD</i>, an Essential Gene in the Tubulin Heterodimer Assembly Pathway is on the source record.

What is the PMID of Infantile Neurodegenerative Disorder Associated with Mutations in<i>TBCD</i>, an Essential Gene in the Tubulin Heterodimer Assembly Pathway?

PICO Portalpmid

The PMID for Infantile Neurodegenerative Disorder Associated with Mutations in<i>TBCD</i>, an Essential Gene in the Tubulin Heterodimer Assembly Pathway is on the source record.

What is the OpenAlex record for Infantile Neurodegenerative Disorder Associated with Mutations in<i>TBCD</i>, an Essential Gene in the Tubulin Heterodimer Assembly Pathway?

PICO Portalopenalex

The OpenAlex for Infantile Neurodegenerative Disorder Associated with Mutations in<i>TBCD</i>, an Essential Gene in the Tubulin Heterodimer Assembly Pathway is on the source record.

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