A novel P3H1 mutation is associated with osteogenesis imperfecta type VIII and dental anomalies
Author:
Funder
Thailand Research Fund
Publisher
Elsevier BV
Subject
Radiology, Nuclear Medicine and imaging,Dentistry (miscellaneous),Pathology and Forensic Medicine,Oral Surgery,Surgery
Reference24 articles.
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3. Emerging Landscape of Osteogenesis Imperfecta Pathogenesis and Therapeutic Approaches;ACS Pharmacology & Translational Science;2024-01-02
4. A Founder Intronic Variant in P3H1 Likely Results in Aberrant Splicing and Protein Truncation in Patients of Karen Descent with Osteogenesis Imperfecta Type VIII;Genes;2023-01-26
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