Mutation analysis ofCOL1A1andCOL1A2in patients diagnosed with osteogenesis imperfecta type I-IV
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Cited by 83 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. From Genetics to Clinical Implications: A Study of 675 Dutch Osteogenesis Imperfecta Patients;Biomolecules;2023-02-02
2. A novel pathogenic variant at the C‐terminal propeptide cleavage site of COL1A1 , causing osteogenesis imperfecta with intrafamilial variability;American Journal of Medical Genetics Part A;2022-03-03
3. Dental Treatment Approach in Two Patients with Osteogenesis Imperfecta: Case Report;Balıkesır Health Sciences Journal;2022-01-03
4. Novel Mutations Within Collagen Alpha1(I) and Alpha2(I) Ligand-Binding Sites, Broadening the Spectrum of Osteogenesis Imperfecta – Current Insights Into Collagen Type I Lethal Regions;Frontiers in Genetics;2021-07-09
5. Toxocara canis Infection Alters lncRNA and mRNA Expression Profiles of Dog Bone Marrow;Frontiers in Cell and Developmental Biology;2021-06-30
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