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A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family

PaperCitations, authors & open-access status

A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family is a paper indexed in ScholarIQ from OpenAlex.

How many citations does A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family have?

ScholarIQcitation count

A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family has 31 citations in the OpenAlex counts ScholarIQ stores.

When was A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family published?

ScholarIQyear

A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family has 2012 year in the ScholarIQ index.

What is the open-access status of A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family?

ScholarIQoa status

A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family has closed oa status in the ScholarIQ index.

What is the DOI of A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family?

ScholarIQdoi

The DOI for A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family is on the source record.

What is the PMID of A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family?

ScholarIQpmid

The PMID for A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family is on the source record.

What is the OpenAlex record for A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family?

ScholarIQopenalex

The OpenAlex for A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family is on the source record.

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