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Genotype/phenotype analysis in Chinese laminin‐α2 deficient congenital muscular dystrophy patients

PaperCitations, authors & open-access status

Genotype/phenotype analysis in Chinese laminin‐α2 deficient congenital muscular dystrophy patients is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Genotype/phenotype analysis in Chinese laminin‐α2 deficient congenital muscular dystrophy patients have?

ScholarIQcitation count

Genotype/phenotype analysis in Chinese laminin‐α2 deficient congenital muscular dystrophy patients has 74 citations in the OpenAlex counts ScholarIQ stores.

When was Genotype/phenotype analysis in Chinese laminin‐α2 deficient congenital muscular dystrophy patients published?

ScholarIQyear

Genotype/phenotype analysis in Chinese laminin‐α2 deficient congenital muscular dystrophy patients has 2014 year in the ScholarIQ index.

What is the open-access status of Genotype/phenotype analysis in Chinese laminin‐α2 deficient congenital muscular dystrophy patients?

ScholarIQoa status

Genotype/phenotype analysis in Chinese laminin‐α2 deficient congenital muscular dystrophy patients has closed oa status in the ScholarIQ index.

What is the DOI of Genotype/phenotype analysis in Chinese laminin‐α2 deficient congenital muscular dystrophy patients?

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The DOI for Genotype/phenotype analysis in Chinese laminin‐α2 deficient congenital muscular dystrophy patients is on the source record.

What is the PMID of Genotype/phenotype analysis in Chinese laminin‐α2 deficient congenital muscular dystrophy patients?

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The PMID for Genotype/phenotype analysis in Chinese laminin‐α2 deficient congenital muscular dystrophy patients is on the source record.

What is the OpenAlex record for Genotype/phenotype analysis in Chinese laminin‐α2 deficient congenital muscular dystrophy patients?

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The OpenAlex for Genotype/phenotype analysis in Chinese laminin‐α2 deficient congenital muscular dystrophy patients is on the source record.

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