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Mutations and clinical characteristics of dRTA caused by SLC4A1 mutations: Analysis based on published patients

PaperCitations, authors & open-access status

Mutations and clinical characteristics of dRTA caused by SLC4A1 mutations: Analysis based on published patients is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Mutations and clinical characteristics of dRTA caused by SLC4A1 mutations: Analysis based on published patients have?

ScholarIQcitation count

Mutations and clinical characteristics of dRTA caused by SLC4A1 mutations: Analysis based on published patients has 12 citations in the OpenAlex counts ScholarIQ stores.

When was Mutations and clinical characteristics of dRTA caused by SLC4A1 mutations: Analysis based on published patients published?

ScholarIQyear

Mutations and clinical characteristics of dRTA caused by SLC4A1 mutations: Analysis based on published patients has 2023 year in the ScholarIQ index.

What is the open-access status of Mutations and clinical characteristics of dRTA caused by SLC4A1 mutations: Analysis based on published patients?

ScholarIQoa status

Mutations and clinical characteristics of dRTA caused by SLC4A1 mutations: Analysis based on published patients has gold oa status in the ScholarIQ index.

What is the DOI of Mutations and clinical characteristics of dRTA caused by SLC4A1 mutations: Analysis based on published patients?

ScholarIQdoi

The DOI for Mutations and clinical characteristics of dRTA caused by SLC4A1 mutations: Analysis based on published patients is on the source record.

What is the PMID of Mutations and clinical characteristics of dRTA caused by SLC4A1 mutations: Analysis based on published patients?

ScholarIQpmid

The PMID for Mutations and clinical characteristics of dRTA caused by SLC4A1 mutations: Analysis based on published patients is on the source record.

What is the OpenAlex record for Mutations and clinical characteristics of dRTA caused by SLC4A1 mutations: Analysis based on published patients?

ScholarIQopenalex

The OpenAlex for Mutations and clinical characteristics of dRTA caused by SLC4A1 mutations: Analysis based on published patients is on the source record.

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