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Clinical Reasoning: A middle-aged man with episodes of gait imbalance and a newly found genetic mutation

PaperCitations, authors & open-access status

Clinical Reasoning: A middle-aged man with episodes of gait imbalance and a newly found genetic mutation is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Clinical Reasoning: A middle-aged man with episodes of gait imbalance and a newly found genetic mutation have?

ScholarIQcitation count

Clinical Reasoning: A middle-aged man with episodes of gait imbalance and a newly found genetic mutation has 2 citations in the OpenAlex counts ScholarIQ stores.

When was Clinical Reasoning: A middle-aged man with episodes of gait imbalance and a newly found genetic mutation published?

ScholarIQyear

Clinical Reasoning: A middle-aged man with episodes of gait imbalance and a newly found genetic mutation has 2012 year in the ScholarIQ index.

What is the open-access status of Clinical Reasoning: A middle-aged man with episodes of gait imbalance and a newly found genetic mutation?

ScholarIQoa status

Clinical Reasoning: A middle-aged man with episodes of gait imbalance and a newly found genetic mutation has bronze oa status in the ScholarIQ index.

What is the DOI of Clinical Reasoning: A middle-aged man with episodes of gait imbalance and a newly found genetic mutation?

ScholarIQdoi

The DOI for Clinical Reasoning: A middle-aged man with episodes of gait imbalance and a newly found genetic mutation is on the source record.

What is the PMID of Clinical Reasoning: A middle-aged man with episodes of gait imbalance and a newly found genetic mutation?

ScholarIQpmid

The PMID for Clinical Reasoning: A middle-aged man with episodes of gait imbalance and a newly found genetic mutation is on the source record.

What is the OpenAlex record for Clinical Reasoning: A middle-aged man with episodes of gait imbalance and a newly found genetic mutation?

ScholarIQopenalex

The OpenAlex for Clinical Reasoning: A middle-aged man with episodes of gait imbalance and a newly found genetic mutation is on the source record.

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