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Unraveling RUNX2 mutation in a cleidocranial dysplasia pa... | ResearchHub
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Unraveling RUNX2 mutation in a cleidocranial dysplasia patient: Molecular insights into osteogenesis and proteostasis
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Authors
Luca Carbonare
14 more
Luca Carbonare
•
Arianna Minoia
12 more
•
Maria Valenti
Published
November 1, 2024
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Journal
Genes & Diseases
Topics
Biology
Cancer Oncology
Medicine
Dentistry
Molecular Biology
Show all topics
DOI
10.1016/j.gendis.2024.101449
License
CC-BY
Supporters
Support the authors with ResearchCoin
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Journal
Genes & Diseases
Topics
Biology
Cancer Oncology
Medicine
Dentistry
Molecular Biology
Show all topics
DOI
10.1016/j.gendis.2024.101449
License
CC-BY
