成骨不全
医学
基因型
儿科
身材矮小
表型
发育不良
人口
遗传学
基因
内科学
病理
生物
环境卫生
作者
Yanfei Luo,Julaiti Dilihuma,Guanghui Sun,Baoerhan Reyilanmu,Ling Liang,Xing-Yue Du,Maimaiti Mireguli
出处
期刊:PubMed
[National Institutes of Health]
日期:2020-02-02
卷期号:58 (2): 135-139
标识
DOI:10.3760/cma.j.issn.0578-1310.2020.02.013
摘要
The cinical phenotypes of osteogenesis imperfecta in Xinjiang Uygur are complex and varied, but all of them have fractures and skeletal deformities. Genotype is different from that reported at China and abroad, and the SERPINF1 gene may have a higher incidence in Uyghur population. The genetic heterogeneity and unique gene variation pedigree of Uyghur osteogenesis imperfecta defects further provide a basis for the correlation between genotype and phenotype of osteogenesis defects.
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