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Characterization of the P373L E-cadherin germline missense mutation and implication for clinical management

PaperCitations, authors & open-access status

Characterization of the P373L E-cadherin germline missense mutation and implication for clinical management is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Characterization of the P373L E-cadherin germline missense mutation and implication for clinical management have?

ScholarIQcitation count

Characterization of the P373L E-cadherin germline missense mutation and implication for clinical management has 55 citations in the OpenAlex counts ScholarIQ stores.

When was Characterization of the P373L E-cadherin germline missense mutation and implication for clinical management published?

ScholarIQyear

Characterization of the P373L E-cadherin germline missense mutation and implication for clinical management has 2007 year in the ScholarIQ index.

What is the open-access status of Characterization of the P373L E-cadherin germline missense mutation and implication for clinical management?

ScholarIQoa status

Characterization of the P373L E-cadherin germline missense mutation and implication for clinical management has closed oa status in the ScholarIQ index.

What is the DOI of Characterization of the P373L E-cadherin germline missense mutation and implication for clinical management?

ScholarIQdoi

The DOI for Characterization of the P373L E-cadherin germline missense mutation and implication for clinical management is on the source record.

What is the PMID of Characterization of the P373L E-cadherin germline missense mutation and implication for clinical management?

ScholarIQpmid

The PMID for Characterization of the P373L E-cadherin germline missense mutation and implication for clinical management is on the source record.

What is the OpenAlex record for Characterization of the P373L E-cadherin germline missense mutation and implication for clinical management?

ScholarIQopenalex

The OpenAlex for Characterization of the P373L E-cadherin germline missense mutation and implication for clinical management is on the source record.

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