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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 PICO Portal from OpenAlex.

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

PICO Portalcitation count

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

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

PICO Portalyear

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

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

PICO Portaloa status

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

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

PICO Portaldoi

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?

PICO Portalpmid

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?

PICO Portalopenalex

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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