ScholarIQanswers from OpenAlex

Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations

PaperCitations, authors & open-access status

Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations have?

ScholarIQcitation count

Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations has 53 citations in the OpenAlex counts ScholarIQ stores.

When was Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations published?

ScholarIQyear

Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations has 2021 year in the ScholarIQ index.

What is the open-access status of Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations?

ScholarIQoa status

Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations has gold oa status in the ScholarIQ index.

What is the DOI of Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations?

ScholarIQdoi

The DOI for Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations is on the source record.

What is the PMID of Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations?

ScholarIQpmid

The PMID for Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations is on the source record.

What is the OpenAlex record for Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations?

ScholarIQopenalex

The OpenAlex for Congenital Diarrhea and Cholestatic Liver Disease: Phenotypic Spectrum Associated with MYO5B Mutations is on the source record.

Related on ScholarIQ

470M+ articles · 14-day free trial