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Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis

PaperCitations, authors & open-access status

Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis have?

ScholarIQcitation count

Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis has 23 citations in the OpenAlex counts ScholarIQ stores.

When was Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis published?

ScholarIQyear

Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis has 2001 year in the ScholarIQ index.

What is the open-access status of Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis?

ScholarIQoa status

Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis has bronze oa status in the ScholarIQ index.

What is the DOI of Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis?

ScholarIQdoi

The DOI for Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis is on the source record.

What is the PMID of Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis?

ScholarIQpmid

The PMID for Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis is on the source record.

What is the OpenAlex record for Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis?

ScholarIQopenalex

The OpenAlex for Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis is on the source record.

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