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 PICO Portal 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 PICO Portal 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 PICO Portal 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 PICO Portal index.

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

The DOI 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 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.