Identification of the CLCN7 gene mutations in two Chinese families with autosomal dominant osteopetrosis (type II)

Identification of the CLCN7 gene mutations in two Chinese families with autosomal dominant osteopetrosis (type II) is a paper indexed in ScholarIQ from OpenAlex.

How many citations does Identification of the CLCN7 gene mutations in two Chinese families with autosomal dominant osteopetrosis (type II) have?

Identification of the CLCN7 gene mutations in two Chinese families with autosomal dominant osteopetrosis (type II) has 32 citations in the OpenAlex counts ScholarIQ stores.

When was Identification of the CLCN7 gene mutations in two Chinese families with autosomal dominant osteopetrosis (type II) published?

Identification of the CLCN7 gene mutations in two Chinese families with autosomal dominant osteopetrosis (type II) has 2009 year in the ScholarIQ index.

What is the open-access status of Identification of the CLCN7 gene mutations in two Chinese families with autosomal dominant osteopetrosis (type II)?

Identification of the CLCN7 gene mutations in two Chinese families with autosomal dominant osteopetrosis (type II) has closed oa status in the ScholarIQ index.

What is the DOI of Identification of the CLCN7 gene mutations in two Chinese families with autosomal dominant osteopetrosis (type II)?

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What is the PMID of Identification of the CLCN7 gene mutations in two Chinese families with autosomal dominant osteopetrosis (type II)?

The PMID for Identification of the CLCN7 gene mutations in two Chinese families with autosomal dominant osteopetrosis (type II) is on the source record.

What is the OpenAlex record for Identification of the CLCN7 gene mutations in two Chinese families with autosomal dominant osteopetrosis (type II)?

The OpenAlex for Identification of the CLCN7 gene mutations in two Chinese families with autosomal dominant osteopetrosis (type II) is on the source record.