Analysis of the clinical and genetic characteristics of a Chinese family with osteogenesis imperfecta type I-Reference-Cited by-同舟云学术

Analysis of the clinical and genetic characteristics of a Chinese family with osteogenesis imperfecta type I

Published:2022-07-19 Issue:9 Volume:10 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Molec Gen & Gen Med

Author:

Niu Zhijie¹,Lai Yongjing¹,Zhou Wenwen¹,Liu Lingyuan¹,Tan Songhua¹,He Guangyao¹,Li Jingyu¹,Tang Fen²,Su Yupei¹,Xu Yanglong¹,Liu Lei¹,Xie Lihong¹,Fang Qin¹,Tang Anzhou¹³^ORCID

Affiliation:

1. Department of Otolaryngology‐Head and Neck Surgery The First Affiliated Hospital of Guangxi Medical University Nanning China

2. Department of Ophthalmology The People's Hospital of Guangxi Zhuang Autonomous region Nanning China

3. Regional Key Laboratory of Early Prevention and Treatment of High‐Rise Tumors Nanning China

Funder

China Postdoctoral Science Foundation

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.2019

Reference18 articles.

1. Mutations in COL1A1 and COL1A2 Genes Associated with Osteogenesis Imperfecta (OI) Types I or III.

2. A novel splicing pathogenic variant inCOL1A1causing osteogenesis imperfecta (OI) type I in a Chinese family

3. DYNAMIC RNA-RNA INTERACTIONS IN THE SPLICEOSOME

4. Osteogenesis imperfecta

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1. Correction to “Analysis of the clinical and genetic characteristics of a Chinese family with osteogenesis imperfecta type I”;Molecular Genetics & Genomic Medicine;2024-08