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Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder

PaperCitations, authors & open-access status

Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder is a paper indexed in PICO Portal from OpenAlex.

How many citations does Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder have?

PICO Portalcitation count

Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder has 47 citations in the OpenAlex counts PICO Portal stores.

When was Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder published?

PICO Portalyear

Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder has 2010 year in the PICO Portal index.

What is the open-access status of Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder?

PICO Portaloa status

Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder has closed oa status in the PICO Portal index.

What is the DOI of Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder?

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The DOI for Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder is on the source record.

What is the PMID of Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder?

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The PMID for Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder is on the source record.

What is the OpenAlex record for Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder?

PICO Portalopenalex

The OpenAlex for Glycogen storage disease type IV: novel mutations and molecular characterization of a heterogeneous disorder is on the source record.

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