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Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect

PaperCitations, authors & open-access status

Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect is a paper indexed in PICO Portal from OpenAlex.

How many citations does Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect have?

PICO Portalcitation count

Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect has 18 citations in the OpenAlex counts PICO Portal stores.

When was Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect published?

PICO Portalyear

Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect has 2018 year in the PICO Portal index.

What is the open-access status of Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect?

PICO Portaloa status

Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect has closed oa status in the PICO Portal index.

What is the DOI of Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect?

PICO Portaldoi

The DOI for Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect is on the source record.

What is the PMID of Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect?

PICO Portalpmid

The PMID for Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect is on the source record.

What is the OpenAlex record for Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect?

PICO Portalopenalex

The OpenAlex for Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect is on the source record.

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