Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect
Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect is a paper indexed in ScholarIQ from OpenAlex.
How many citations does Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect have?
Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect has 18 citations in the OpenAlex counts ScholarIQ stores.
When was Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect published?
Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect has 2018 year in the ScholarIQ index.
What is the open-access status of Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect?
Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect has closed oa status in the ScholarIQ index.
What is the DOI of Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect?
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What is the PMID of Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect?
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The OpenAlex for Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect is on the source record.